Glossary of health conditions
This glossary provides definitions and information on various health conditions affecting the human body. It serves as a quick reference for understanding these conditions.
A[edit | edit source]
- Asthma - A chronic respiratory condition marked by spasms in the bronchi of the lungs, causing difficulty in breathing.
- Alzheimer's Disease - A progressive neurodegenerative disease that causes memory loss and cognitive decline.
B[edit | edit source]
- Bronchitis - Inflammation of the lining of bronchial tubes, which carry air to and from the lungs.
- Bipolar Disorder - A mental disorder causing periods of depression and periods of abnormally elevated mood.
C[edit | edit source]
- Cancer - A disease caused by an uncontrolled division of abnormal cells in a part of the body.
- Celiac Disease - An immune reaction to eating gluten, a protein found in wheat, barley, and rye.
D[edit | edit source]
- Diabetes - A group of diseases that result in too much sugar in the blood (high blood glucose).
- Dyslexia - A learning disorder characterized by difficulty reading due to problems identifying speech sounds and learning how they relate to letters and words.
E[edit | edit source]
- Epilepsy - A neurological disorder marked by sudden recurrent episodes of sensory disturbance, loss of consciousness, or convulsions, associated with abnormal electrical activity in the brain.
- Endometriosis - A painful disorder in which tissue similar to the tissue that normally lines the inside of your uterus — the endometrium — grows outside your uterus.
F[edit | edit source]
- Fibromyalgia - A chronic condition characterized by widespread musculoskeletal pain, fatigue, and tenderness in localized areas.
- Fatty Liver Disease - A condition where excess fat builds up in the liver.
G[edit | edit source]
- Gastroesophageal Reflux Disease (GERD) - A digestive disease in which stomach acid or bile irritates the food pipe lining.
- Glaucoma - A group of eye conditions that can cause blindness by damaging the nerve at the back of the eye (optic nerve).
H[edit | edit source]
- Hypertension - Also known as high blood pressure, a condition in which the blood vessels have persistently raised pressure.
- HIV/AIDS - Human Immunodeficiency Virus/Acquired Immune Deficiency Syndrome, a spectrum of conditions caused by infection with the HIV virus.
I[edit | edit source]
- Influenza - A viral infection that attacks your respiratory system — your nose, throat, and lungs.
- Irritable Bowel Syndrome (IBS) - An intestinal disorder causing pain in the belly, gas, diarrhea, and constipation.
J[edit | edit source]
- Jaundice - Yellowing of the skin and whites of the eyes caused by an accumulation of bilirubin in the blood.
K[edit | edit source]
- Kidney Stones - Hard deposits made of minerals and salts that form inside your kidneys.
L[edit | edit source]
- Leukemia - A type of cancer of the blood or bone marrow characterized by an abnormal increase of white blood cells.
- Lupus - A systemic autoimmune disease that occurs when your body's immune system attacks your own tissues and organs.
M[edit | edit source]
- Migraine - A headache of varying intensity, often accompanied by nausea and sensitivity to light and sound.
- Multiple Sclerosis - A disease in which the immune system eats away at the protective covering of nerves.
N[edit | edit source]
- Nephritis - Inflammation of the kidneys that can lead to kidney failure.
- Neuropathy - Damage or dysfunction of one or more nerves, typically causing numbness or weakness.
O[edit | edit source]
- Osteoporosis - A medical condition in which the bones become brittle and fragile from loss of tissue.
P[edit | edit source]
- Parkinson's Disease - A progressive nervous system disorder that affects movement.
- Psoriasis - A skin disease that causes red, itchy scaly patches, most commonly on the knees, elbows, trunk, and scalp.
Q[edit | edit source]
- Quadriplegia - Paralysis of all four limbs; tetraplegia.
R[edit | edit source]
- Rheumatoid Arthritis - A chronic inflammatory disorder affecting many joints, including those in the hands and feet.
S[edit | edit source]
- Stroke - Damage to the brain from interruption of its blood supply.
- Scoliosis - A sideways curvature of the spine that occurs most often during the growth spurt just before puberty.
T[edit | edit source]
- Tuberculosis - A potentially serious infectious bacterial disease that mainly affects the lungs.
- Tinnitus - Ringing or buzzing noise in one or both ears that may be constant or come and go, often associated with hearing loss.
U[edit | edit source]
- Ulcerative Colitis - A chronic, inflammatory bowel disease that causes inflammation in the digestive tract.
- Urticaria - Also known as hives, a rash of round, red welts on the skin that itch intensely, sometimes with dangerous swelling.
V[edit | edit source]
- Varicella - Also known as chickenpox, a highly contagious disease caused by the initial infection with varicella zoster virus.
W[edit | edit source]
- Whooping Cough - Also known as pertussis, a highly contagious respiratory tract infection.
X[edit | edit source]
- Xerophthalmia - A medical condition in which the eye fails to produce tears.
Y[edit | edit source]
- Yellow Fever - A viral infection spread by a particular species of mosquito.
Z[edit | edit source]
- Zika Virus - A disease caused by Zika virus that's spread through mosquito bites.
Terms that need improvement[edit | edit source]
- ACTH (Adrenocorticotropic hormone) deficiency - Too little ACTH produced by the pituitary.
- ACTH (Adrenocorticotropic hormone) - Hormone produced by the pituitary gland. It stimulates.
- AIDS (Acquired Immune Deficiency Syndrome) - Major failure of body's immune system.
- Abell-Kendall modification - Modification of a lab test developed by Drs. Abell and Kendall.
- Abruptio placenta - Separation of the placenta from the uterus during the last trimester of pregnancy.
- Abscess - Swollen, inflamed, tender area of infection filled with pus.
- Achalasia - Condition of the esophagus that disrupts normal swallowing.
- Acid-base imbalance - Imbalance that occurs when body retains too much acid or too much base.
- Acidosis, metabolic - Too much acid in the body due to loss of base.
- Acidosis, respiratory - Too much acid in the body due to accumulation of excess carbon dioxide.
- Acidosis - Pathologic condition resulting from accumulation of too much acid in the body.
- Acromegaly - Condition that afflicts middle-aged people. Characterized by a gradual, marked.
- Acute intermittent porphyria (AIP) - Disease of porphyrin metabolism. Symptoms include recurrent.
- Acute pulmonary edema - Set of dramatic, life-threatening symptoms, including extreme shortness of.
- Acute - Beginning suddenly. Severe but of short duration.
- Addison's disease (Adrenal insufficiency) - Condition caused by inactive or underactive adrenal.
- Adenocarcinoma - Any of a large group of cancerous tumors of a gland or gland tissue.
- Adenoma - Benign tumor of glandular cells. May cause excess hormone secretion by the affected.
- Adhesions - Small strands of fibrous tissue that cause organs in the abdomen and pelvis to cling.
- Adrenal cortex - Outer layer of the adrenal gland. Secretes various hormones including cortisone.
- Adrenal hyperplasia - Abnormal increase in the number of normal cells in the adrenal gland(s).
- Adrenal insufficiency - See Addison's disease.
- Adrenal medulla tumors (Pheochromocytoma) - Tumors of the medulla, an inner layer of the adrenal.
- Adrenal medulla - Middle part of the adrenal gland. Secretes epinephrine (adrenalin) and.
- Adrenal - Pertaining to one or both glands located adjacent to the kidneys. These glands secrete many.
- Adrenocortical hyperplasia - Increase in the number of cells of the adrenal cortex. Adrenal cortex.
- Adrenocorticotropic hormone deficiency - Not enough ACTH is produced by the pituitary gland.
- Adrenoleukodystrophy - Disturbance in brain substance caused by abnormal function of the adrenal.
- Agglutination - Clumping together.
- Ahaptoglobulinemia - Without haptoglobin in the blood. Condition is often seen with hemolytic.
- Alcohol cardiomyopathy - Disease of the myocardium (muscle layer) of the heart, due to chronic.
- Alcoholic polymyopathy - Disease affecting several muscles simultaneously. Caused by alcoholism.
- Aldosteronism, primary - Overproduction of aldosterone, which is secreted by adrenal glands.
- Alkalosis, metabolic - Abnormal condition in which body fluids are more alkaline than normal. Can.
- Alkalosis, respiratory - abdominal pain, diarrhea, appetite loss and brown skin. Abnormal condition.
- Alveolar edema - Swelling of the smallest branches of the bronchial tubes (alveoli).
- Ambiguous genitalia - External genitals that are not normal for the sex.
- Amblyopias - Reduced vision in an eye that appears to be normal when examined with an.
- Amenorrhea - There are two categories of amenorrhea. In primary amenorrhea, menstruation has not.
- Amine - Organic chemical compound containing nitrogen.
- Amino acids - Organic chemical compounds. They are the chief components of all proteins. The body.
- Ampulla of Vater - Enlarged area where the pancreatic duct and common bile duct come together.
- Amyloid infiltration - See Amyloidosis.
- Amyloid - Starchy substance.
- Amyloidosis - Disease in which a waxy, starchlike, translucent material accumulates in tissues and.
- Amyotrophic lateral sclerosis (ALS; Lou Gehrig's disease) - Progressive breakdown of spinal.
- Anaphylaxis (Allergic shock) - Severe,life-threatening allergic response to medications or other.
- Andrenogenital syndrome - Endocrine disorder resulting from adrenocortical hyperplasia. See.
- Androgenic arrhenoblastoma - Ovarian tumor in which cells resemble.
- Anemia, aplastic - Serious disease characterized by decreased bone marrow production of all blood.
- Anemia, autoimmune hemolytic - Anemia due to the breakdown of an individual's blood cells by his.
- Anemia, chronic hemolytic - Anemia caused by an inherited disorder, such as hereditary.
- Anemia, diserythropoietic - Any anemia caused by a disorder that diminishes the body's normal.
- Anemia, hemolytic - Anemia due to the premature destruction of mature red blood cells. Bone.
- Anemia, hypochromic - Any of a large group of anemias characterized by a decreased concentration.
- Anemia, hypoplastic - Anemia characterized by decreased bone marrow production of red blood.
- Anemia, idiopathic acquired hemolytic - Anemia characterized by a shortened lifespan of red blood.
- Anemia, iron deficiency - Decreased number of circulating red blood cells or insufficient hemoglobin.
- Anemia, macrocytic - Blood disorder characterized by abnormal presence of large, fragile red blood.
- Anemia, megalobastic (Folic acid deficiency) - Anemia caused by folic acid deficiency. Often.
- Anemia, microcytic - Any anemia characterized by abnormally small red blood cells, usually.
- Anemia, non-spherocytic hemolytic - Inherited disorder of red blood cells in which shortened red.
- Anemia, pernicious - Anemia caused by inadequate absorption of vitamin B12.
- Anemia, pyridoxine-responsive - Decreased red blood cells in circulation, which increase to normal.
- Anemia, sickle cell trait - See Sickle cell trait.
- Anemia, sickle cell - Severe, incurable anemia that occurs in people who have an abnormal form of.
- Anemia, sideroblastic -A special type of anemia in which the bone marrow deposits iron prematurely into red blood cells. These cells do not transport oxygen to the body as efficiently as normal cells.
- Anemia - Condition in which the number of red blood cells or hemoglobin (oxygen carrying substance.
- Anencephaly - Absence of the brain.
- Aneuploidy - Any variation in chromosome number that involves individual chromosomes and not.
- Aneurysm - Abnormal enlargement or ballooning of an artery. Caused by a weak artery wall.
- Angina (Angina pectoris) - Chest pain or pressure usually beneath the sternum (breastbone). Caused.
- Angina pectoris - See Angina.
- Angiodysplasia - Small blood vessel abnormalities.
- Angioedema (Angioneurotic edema; hives) - Allergic disorder characterized by skin changes with.
- Angiomas - Benign tumor made up of blood vessels or lymph vessels. Most are congenital.
- Anion gap - Measure combining laboratory analysis of sodium, chloride and bicarbonate. A quick.
- Ankylosing spondylitis - Chronic, progressive disease of the joints, accompanied by inflammation and.
- Anorectal abscess - Abscess occurring in the rectum (last segment of the large intestine) and anus.
- Anorexia nervosa - Extremely complicated personality disorder, chiefly in young women.
- Anorexia - Loss of appetite.
- Anti-lipemic (Anti-lipidemic) - Of or pertaining to a regimen, diet, agent or drug that reduces the.
- Antigens - Germs or other sources of disease that antibodies (produced by the immune system).
- Antinuclear antibody (ANA) - Substance that appears in the blood indicating presence of an.
- Aortic-valve stenosis - Heart abnormality characterized by narrowing or stricture of the aortic valve.
- Aortoiliac occlusive disease - Complete or partial blocking of the lower part of the aorta as it enters.
- Aplastic anemia - See Anemia, aplastic.
- Apnea - Absence of spontaneous breathing.
- Appendicitis - Inflammation of the vermiform appendix (small tube that extends from the first part of.
- Arachnoiditis - Inflammation of the arachnoid membrane, a thin, delicate membrane enclosing the brain.
- Arginosuccinic aciduria - Presence of arginosuccinic acid in the urine. This is an inborn error of.
- Arrhythmias - Occasional or constant abnormalities in the rhythm of the heartbeat.
- Arterial-occlusive disease - Total or partial blockage of any large artery.
- Arteriosclerosis - Common disorder of the arteries characterized by thickening, loss of elasticity and.
- Arteriovenous malfunction - Problem at the junction of an artery and vein at the capillary level.
- Arthritis - Inflammatory condition of the joints, characterized by pain and swelling. Also see.
- Ascites - Accumulation of serous fluid in the abdominal cavity. It contains large amounts of protein and.
- Asphyxia - Loss of consciousness due to too little oxygen and too much carbon dioxide in the blood. If.
- Asthma - Chronic disorder with recurrent attacks of wheezing and shortness of breath.
- Astigmatism - Visual impairment caused by abnormal eye shape.
- Astrocytomas - Brain tumor composed of neuroglial cells (one of the two main kinds of cells that make.
- Ataxia-telangiectasia - Severe, hereditary, progressive disease beginning in early childhood. It results.
- Atopic dermatitis - Chronic inflammatory disease of the skin; often associated with other allergic.
- Atria - Chamber allowing entrance into another structure. Usually refers to ATRIA of the heart, which.
- Atrial fibrillation - Completely irregular heartbeat rhythm. In this case, it occurs in the top chambers of.
- Atrophy - Wasting away; diminishing in size such as a cell, tissue, organ or part. May result from.
- Autoimmune disease - Disease in which the immune system produces antibodies that attack the.
- Autoimmune hemolytic anemia - See Anemia, autoimmune hemolytic.
- Autoimmune thyroid disease - See Grave's disease.
- Autoimmune - Response directed against the body's own tissue.
- B-Thalassemia - Hemolytic anemia caused by decreased production of beta chains of hemoglobin in.
- BILE SAND - Thickened, gritty bile excreted by the liver into the gallbladder and bile ducts. Bile sand.
- Bacteremia - Presence of bacterial germs in the bloodstream.
- Bacterial endocarditis - Noncontagious infection of the valves or lining of the heart.
- Bacterial myocarditis - Infection of the heart muscle caused by bacterial germs.
- Baker's cyst - Benign tumor on the back of the knee joint. Tumor consists of accumulated fluid that.
- Bartter's syndrome - Inherited disease characterized by short stature, mental retardation.
- Benign - 1) Tumor or growth that is neither cancerous nor located where it might impair normal.
- Bernard-Soulier syndrome - Hereditary coagulation disorder marked by a mild decrease in the.
- Beta-blockers - Medications that reduce heart or blood vessel overactivity to improve blood.
- Biliary obstruction - Blockage of the common or cystic bile duct, usually by one or more gallstones.
- Bilirubin, unconjugated - Bilirubin that is insoluble in water. Bilirubin normally travels in the.
- Bilirubin - Yellowish red blood cell waste product in bile the blood carries to the liver. It contributes to.
- Biopsy - Removal of a small amount of tissue or fluid for laboratory examination; aids in diagnosis.
- Bitemporal hemianopsic - Defective vision in which blindness occurs in the outer half of the visual field.
- Blastic phase - Immature stage of cell development.
- Blastomycosis - Infectious fungal disease that starts in the lungs. Occasionally it spreads through the.
- Blood dyscrasias - Condition caused by or relating to disease in which any component of the blood is.
- Blood-factor deficiency - Deficiency of one of the blood factors. See Factor I through Factor XIII.
- Blood - Liquid pumped by the heart through arteries, veins and capillaries. It consists of a clear, yellow.
- Bone disorders - Any abnormality or disease of the bone or skeletal system.
- Bone marrow disease - Any disease affecting bone marrow. See Bone marrow.
- Bone marrow - Specialized soft tissue that fills the core of bones. Most of the body's red and white.
- Botulism - Serious form of food poisoning caused by eating contaminated food containing a toxin that.
- Brain infarctions - Localized area of brain tissue death resulting from lack of oxygen to that area.
- Bronchial tubes (Bronchi) - Hollow air passageways that branch from the windpipe (trachea) into the.
- Bronchiectasis - Lung disease in which bronchial tubes become blocked and accumulate thick.
- Bronchitis - Acute or chronic inflammation of the bronchial tubes. Acute bronchitis is usually caused by.
- Bronchodilator - Any member of a group of drugs that dilates bronchial tubes and makes air passage.
- Bronchogenic carcinoma - Malignant tissue growth in the lung, which may be caused by cigarette.
- Brucellosis (Undulant fever) - Illness caused by the brucella bacteria, which is transmitted to humans.
- Cachexia - General poor health and malnutrition, including weakness and muscle wasting. Usually.
- Calcification - Process by which calcium from the blood is deposited abnormally into tissues from.
- Calcium disorders - Imbalance in the amount of calcium in the blood. Too much or too little can cause.
- Calcium - Component of blood that helps regulate the heartbeat, transmit nerve impulses, contract.
- Calculi - Stones formed of mineral salts. Usually found within hollow organs or ducts. They can cause.
- Cancer - See Carcinoma.
- Cannula - Tube for insertion into a vessel or body cavity.
- Capillary precipitation - Settling of solid substances formerly in solution in the bloodstream.
- Capillary - Smallest blood vessels in the body.
- Carcinoma - Malignant tumor that tends to invade surrounding tissue; it may travel to distant regions of.
- Cardiac distress - Any condition causing difficulty in heart's normal functioning.
- Cardiac glycosides - Family of drugs used to treat heart disease. Digitalis is the outstanding cardiac.
- Cardiac tamponade - Compression of the heart due to collection of blood in the sac enclosing the.
- Cardiomyopathy (Hypertrophic cardiomyopathy) - Disorder of the heart muscle usually associated.
- Cardiorespiratory disease (Cardiopulmonary disease) - Any disease affecting the heart and lungs.
- Cardioversion - Restoration of normal rhythm of the heart by electrical shock.
- Casts - Gelled protein particles on the walls of kidney tubules that break off and are washed out by.
- Cataracts - Clouding of the eye lens. A common cause of vision loss. Most commonly occurs in.
- Catheter - Hollow tube used to introduce fluids into the body or to drain fluids from the body.
- Cation-anion - Positively charged ion attracted to the positive electrode in electrolysis.
- Celiac disease (Nontropical sprue) - Congenital disorder caused by an intolerance for gluten, a.
- Cephalopelvic disproportion (CPD) - Obstetric condition in which an infant's head is too large or the.
- Cervical spondylosis - Degenerative changes of bones in the neck that place pressure on nerves and.
- Cervix - Lower third of the uterus, which protrudes into the vagina.
- Charcot's disease (Neuropathic joint disease) - Chronic, progressive degeneration of a joint, which.
- Chemical inhibition - Process of retarding, arresting or restraining a chemical reaction.
- Chemical profile (SMAC) - Cost is about $24.00. This profile of tests is performed on an electronic.
- Chemotherapy - Treatment of cancer with medication that kills cancer cells without harming healthy.
- Cholangitis - Infection or inflammation of the bile ducts (biliary tract) that drain bile from the.
- Cholecystitis - Gallbladder inflammation usually caused by a gallstone that cannot pass through the.
- Choledocholithiasis (Biliary calculus; biliary stone) - Stone formed in the biliary tract. See Kidney.
- Cholelithiasis (Gallstone) - Stones in the gallbladder that may or may not cause symptoms. If.
- Cholestasis intrahepatic - Interruption in the flow of bile to the biliary tract. May be caused by.
- Chondromalacia patellae - Occurs after knee injury. Characterized by swelling, pain and degenerative.
- Chondromalacia - Abnormal softening of cartilage.
- Choriocarcinoma - Malignancy arising in the uterus associated with pregnancy, abortion or.
- Christmas disease - See Hemophilia.
- Chromatin mass - Portion of the cell nucleus that carries the genes of inheritance.
- Chromophobe adenoma - Tumor of the anterior portion of the pituitary gland; cells do not stain with.
- Chromosome - Structures inside the nucleus of living cells that contain hereditary information. Defects.
- Chronic bronchitis - Inflammation caused by repeated irritation or infection of the bronchial tubes.
- Chronic - Long-term; continuing. Chronic illnesses are usually not curable, but they can often be.
- Chyle - Lymph and droplets of triglyceride fat in a stable emulsion. See Lymph. Lymph forms a milky.
- Circle of Willis - Network of blood vessels at the base of the brain, formed by the interconnection of.
- Cirrhosis - Chronic scarring of the liver, leading to loss of normal liver function.
- Citrullinuria - Presence of large amounts of citrulline in the urine, plasma and cerebrospinal fluid.
- Coagulation defects (Coagulopathy) - Disruption of blood clotting mechanisms, resulting in.
- Coagulation factors - Chemical compounds necessary for blood to clot. See Factor I through Factor.
- Coccidioidomycosis (Valley fever) - Infection caused by breathing spores of a fungus found in soil. It.
- Cold agglutinins - Antibodies that cause red blood cells to clump together at low temperatures.
- Colitis - Inflammatory condition of the large intestine. It can occur in episodes, such as irritable bowel.
- Collagen disease - See Connective tissue disease.
- Collagen-vascular disease - See Connective tissue disease.
- Collagen-vascular-autoimmune disease - See Autoimmune disease. Examples of this disease are.
- Complement - Series of enzymes in normal blood that interacts with antigens and antibodies.
- Condyloma - Wart-like growth on the mucous membrane or skin of the external genitals or around the.
- Congenital anomalies - Abnormality of the body present at birth; a birth defect. May be inherited or.
- Congenital hypothyroidism (Cretinism) - Deficiency or lack of thyroid hormone secretion during.
- Congenital - Present at, and existing from, the time of birth.
- Congestive heart failure - Complication of many serious diseases in which the heart loses its full.
- Conjunctivitis - Inflammation of the lining of the eyelids and the covering of the white part of the eye.
- Conn's syndrome - Disorder of the adrenal cortex. See Adrenal cortex. Usually a noncancerous tumor.
- Connective-tissue disease (Collagen disease) - Any one of many abnormal conditions.
- Coproporphyria - See Porphyria.
- Corneoscleral flaccidity - Abnormal softness of the cornea and sclera of the eye.
- Corneoscleral rigidity - Abnormal inflexibility of the cornea and sclera of the eye.
- Coronary artery bypass surgery - Using a section of the patient's leg vein to bypass a partial or.
- Coronary artery disease - Hardening and narrowing of the coronary arteries that provide blood to the.
- Coronary insufficiency - Condition of the main arteries in the heart in which they supply an insufficient.
- Coronary occlusion - Hardening and narrowing of one or more of the coronary arteries that provide.
- Coronary-risk profile - Cost is about $40.00. Blood tests performed include Total Cholesterol, page.
- Craniopharyngiomas - Congenital pituitary tumor appearing most often in children and adolescents.
- Creatinine - Substance formed from the metabolism of creatine, which is found in blood, urine and.
- Crepitus - Crunching sound similar to the sound made when tissue paper is crushed.
- Cretinism - Deficiency of thyroid hormone secretion during fetal development or early infancy. In.
- Crohn's disease (Regional enteritis) - Inflammation of any part of the gastrointestinal tract that.
- Cryoglobulins - Abnormal blood proteins that separate from blood at low laboratory temperatures and.
- Crystal-induced arthritis - Inflammation of a joint characterized by crystallization of fluids in a joint.
- Cushing's disease (Cushing's syndrome) - Condition due to tumors of the adrenal cortex or the.
- Cushing's syndrome - See Cushing's disease.
- Cyanosis - Bluish discoloration of skin, lips and nails. Caused by lack of oxygen.
- Cyst - Sac or cavity filled with fluid or disease matter.
- Cystic fibrosis - Inherited disease in which mucus-producing glands throughout the body, especially in.
- Cystic tumors - Tumors with cavities or sacs containing a semisolid or liquid material.
- Cystinuria - Abnormal presence of cystine (an amino acid) in the urine. Also inherited defect in the.
- Cytomegalovirus (CMV) infection - Viral infection caused by cytomegalovirus. Characterized by.
- Cytotoxic agents - Medications used to destroy cancerous cells with minimal harm to healthy cells.
- Cytotoxic - Having a negative effect upon cells.
- DIC - See Disseminated intravascular coagulation.
- DUMPING SYNDROME - Group of symptoms that is a complication of surgical removal of all or.
- Delirium tremens (DTs) - Acute, sometimes fatal, psychotic reaction caused by excessive intake of.
- Demyelinating disease - Outer wrapping (myelin sheath) of the nerves or nerve fibers is destroyed.
- Dermatitis - Inflammatory condition of the skin, characterized by redness and pain or itching. The type.
- Dermatofibromas - Fibrous, tumorlike nodule of the skin most commonly found on the arms or legs.
- Dermatomyositis - Inflammation of connective tissue, with degenerative changes in muscles and skin.
- Detached retina - Separation or tear of the light-sensitive tissue at the back of the eye (retina) from the.
- DiGeorge's syndrome - Congenital disorder characterized by severe immunodeficiency, birth defects.
- Diabetes insipidus - Disorder of the hormone system caused by a deficiency of antidiuretic hormone.
- Diabetes mellitus: Insulin dependent - Inability to produce enough insulin to process carbohydrates.
- Diabetes mellitus: Non-insulin dependent - Disease of metabolism characterized by the body's.
- Diabetes - Any of various diseases characterized by an excessive discharge of urine.
- Diabetic acidosis - See Diabetic ketoacidosis.
- Diabetic ketoacidosis - Serious complication of diabetes mellitus in which the body produces acids.
- Diabetic retinopathy - Disorder of the innermost coat of the back of the eyeball. Seen most frequently.
- Dialysis - Process of separating crystals and other substances in a solution by the difference in their.
- Diaphoresis - Profuse perspiration.
- Diaphragm - Large, thin muscle that separates the chest cavity from the abdominal cavity.
- Diaphragmatic paralysis - Complete loss of function of the diaphragm. See Diaphragm. The.
- Diphtheria - Highly contagious infection, primarily affecting the mucous membranes of the nose, throat.
- Diploidy - Having two full sets of chromosomes.
- Disease - Process representing a departure from normal health.
- Diserythropoietic anemia - See Anemia, diserythropoietic.
- Disseminated intravascular coagulation - Serious disruption of blood clotting mechanisms, resulting.
- Diverticula - Small, pouch-like projections in the wall of the colon.
- Diverticulitis - Inflammation of diverticula. During periods of inflammation, person experiences crampy.
- Down's syndrome - Condition associated with a chromosome abnormality, usually trisomy of.
- Duchenne muscular dystrophy - Abnormal congenital condition characterized by progressive.
- Duodenal lesions - Abnormalities in the duodenum, such as ulcers, tumors or inflammatory reactions.
- Duodenal ulcer - Peptic ulcer located in the duodenum, which is the first segment (about 10-inches.
- Duodenitis - Inflammation of mucous membrane lining of the duodenum.
- Duodenum - First portion of the small intestine.
- Dwarfism - Underdevelopment of the body.
- Dysentery - Inflammation of the intestine, especially the colon; may be caused by chemical irritants.
- Dysfibrinogenemia - Congenital disorder in which fibrinogen is present in the blood, but does not.
- Dyspnea - Difficulty breathing.
- Dysproteinemia - Derangement of the protein content of the blood.
- Eclampsia (Toxemia of pregnancy) - Extremely serious disturbance in blood pressure, kidney.
- Ectopic ACTH production - Adrenocorticotropic hormone production (ACTH) at some site other.
- Ectopic pregnancy - Pregnancy that develops outside the uterus. The most common site is one of the.
- Edema - Accumulation of fluid under the skin (swelling), in the lungs or elsewhere.
- Electrolyte package - Cost is about $20.00. Blood tests performed include Sodium, page 184.
- Elliptocystosis - Hereditary disorder in which red blood cells (erythrocytes) are oval in shape, instead.
- Embolism - Sudden blockage of a blood vessel by an embolus. See Embolus.
- Embolus - Clot, foreign object, air, gas or a bit of tissue or fat that circulates in the bloodstream until it.
- Encephalitis - Acute inflammation of the brain, usually caused by a contagious viral infection. May also.
- Endobronchial - Within the bronchial tubes.
- Endocrine disorders - Any disorder involving the endocrine system. The endocrine system is made up.
- Endometriosis - Disorder in women in which tissue resembling inner lining of the uterus (endometrium).
- Enteritis - Inflammation of the mucous membrane lining of the small intestine.
- Enterocolitis - Inflammation of the mucous membrane lining of the small and large intestine.
- Ependymomas - Tumor in the brain or spinal cord that is usually benign and slow growing.
- Epilepsy, focal - Small part of the body begins twitching uncontrollably. The twitching (seizure).
- Epilepsy, grand mal - Affects all ages. Person loses consciousness, stiffens, then twitches and jerks.
- Epilepsy, petit mal - Affects children mostly. Child stops activity and stares blankly around for a.
- Epilepsy, temporal lobe - Person suddenly behaves out of character or inappropriately, such as.
- Epilepsy - Disorder of brain function. There are several forms of epilepsy, each with its own.
- Erythroblastosis fetalis (Rh-incompatibility) - Incompatibility between an infant's blood type and.
- Erythropoiesis - Formation of red blood cells.
- Erythropoietic porphyrias - Inherited disorder in which there is an abnormal increase in the.
- Erythropoietic protoporphyrias - Disease characterized by itching, redness and edema after short.
- Esophageal rings - Muscular fibers that surround the esophagus.
- Esophageal varices - Enlarged veins on the lining of the esophagus subject to severe bleeding. They.
- Esophagitis - Inflammation of the mucous-membrane lining of the esophagus. May be caused by.
- Esophagus - Hollow tube that provides passage from the back of the throat to the stomach.
- Essential hypertension - See Hypertension.
- Eunuchoidism - Deficiency of male hormone, which results in abnormal tallness, small testes and.
- Exchange transfusion - Introduction of whole blood in exchange for 75 to 85% of an infant's.
- Exudate - Matter that penetrates through vessel walls into adjoining tissue. Production of pus or serum.
- FSP (Fibrin split products) - Results from the breakdown of fibrinogen by plasmin (an enzyme). See.
- Factor III - Tissue thromboplastin needed for blood to clot.
- Factor II - Prothrombin needed for blood to clot.
- Factor IV - Calcium needed for blood to clot.
- Factor IX - Plasma thromboplastin component needed for blood to clot.
- Factor I - Fibrinogen needed for blood to clot.
- Factor VIII - Anti-hemophilic factor needed for blood to clot.
- Factor VII - Proconvertin needed for blood to clot.
- Factor VI - Accelerin needed for blood to clot.
- Factor V - Proaccelerin needed for blood to clot.
- Factor XIII - Fibrin-stabilizing factor needed for blood to clot.
- Factor XII - Hageman factor needed for blood to clot.
- Factor XI - Plasma thromboplastin antecedent needed for blood to clot.
- Factor X - Stuart factor (autoprothrombin C) needed for blood to clot.
- Factor-VII deficiency - Deficiency of normal clotting factor. Can be inherited or acquired. This.
- Familial hypoproteinemia - Inherited abnormal decrease in the amount of protein in the blood.
- Familial myoglobinuria - Inherited condition in which myoglobin appears in urine. Causes include.
- Familial xanthurenic aciduria - Inherited deficiency disorder of xanthine oxidase that causes physical.
- Fanconi's syndrome - Rare, usually congenital disorder characterized by aplastic anemia, bone.
- Fetal hypoxia - Absence of sufficient oxygen to sustain life in a fetus.
- Fibrillation - Quivering of heart muscle fibers.
- Fibrin split products - See FSP.
- Fibrin - Protein formed from fibrinogen by the action of blood clotting.
- Fibrinogen - Protein in the blood needed for blood clotting.
- Fibrinolysis, secondary - Process by which connective tissue is dissolved by the action of enzymes as.
- Fibrinolysis, systemic - See Fibrinolytic disorders.
- Fibrinolysis - Breakdown of fibrin by enzyme action.
- Fibrinolytic disorders - Disease process characterized by dissolution of connective tissue by the action.
- Fibrocystic disease (Breast lumps) - Disorder of the female breast characterized by nonmalignant.
- Fibroids - Abnormal growth of cells in the muscular wall of the uterus (myometrium). Uterine fibroids.
- Fibromas - Benign neoplasm of fibrous or fully developed connective tissue.
- Fibrosis - Generation of fibrous tissue, such as in a scar.
- Fibrous ankylosis - Immobility and consolidation of a joint from disease caused by fibrous tissue.
- Fibrous tissue - Tissue that is made up of fibers.
- Filariasis - Disease caused by the presence of parasitic worms or larvae in body tissue. Worms are.
- Fissures - 1) Cleft or groove on the surface of an organ, often marking division of the organ into parts.
- Fistulas - Abnormal passage between two organs or between an internal organ and the body surface.
- Fluoresce - Emits light while exposed to light.
- Focal epilepsy - See Epilepsy, focal.
- Focal seizures - Convulsions brought about by a disease process or injury to an identifiable part of the.
- Fulminating infection - Infection that occurs suddenly, with great intensity.
- G-6-PD (Glucose-6-phosphate dehydrogenase) - Enzyme normally found in most body cells.
- Galactorrhea - Breast milk flow not associated with childbirth or breast feeding. It may be a symptom.
- Galactosemia - Inherited disease of infants in which milk cannot be digested. Milk should be eliminated.
- Gallbladder disease - Any disease involving the gallbladder or biliary tract. The gallbladder is a.
- Gallstones - Calculus or stone formed in the gallbladder. See Cholelithiasis.
- Ganglioneuroblastoma - Tumor of nerve cells.
- Ganglioneuroma - Benign tumor composed of nerve fibers.
- Gangrene - Dead tissue. Develops when a wound becomes infected or tissue is destroyed by an.
- Gastrin - Hormone that stimulates the production of gastric acid or stomach acid.
- Gastrinoma - Benign or malignant gastrin-secreting islet-cell tumor of the pancreas. There is an.
- Gastritis - Irritation, inflammation or infection of the stomach lining. Cause is sometimes unknown but.
- Gastroenteritis - Inflammation of the stomach and intestines accompanying many digestive-tract.
- Gastrointestinal (GI) symptoms - Any symptoms relating to the stomach or intestine. Some common.
- Gastrointestinal disease - Any disorder of the gastrointestinal tract, which includes the mouth.
- Gastrointestinal disorders - Any condition or disease relating to any part of the digestive system.
- Gaucher's disease - Rare familial disorder of fat metabolism characterized by an enlarged spleen.
- Genital herpes - Viral infection of the genitals transmitted by intercourse or oral sex. Genital herpes.
- Germ cell tumors - One of three types of cancer of the ovary. Arises in the ovum (egg). Prognosis is.
- Gigantism - Condition in which the body or a body part grows excessively, sometimes due to an.
- Gilbert's disease (Gilbert's syndrome) - Benign hereditary condition characterized by jaundice and.
- Glanzmann's thrombosthemia - Rare, inherited hemorrhagic disease. See Hemorrhagic disease.
- Glaucoma - Abnormally increased pressure within the eyeball that may produce severe, permanent.
- Globulins - Class of proteins that are insoluble in water but soluble in saline solutions.
- Glomerular - Of or pertaining to a glomerulus.
- Glomerulonephritis (Post-infectious, acute or chronic) - Inflammation of glomerulus. See.
- Glomerulus - Tiny structure composed of blood vessels. One of several structures that make up a.
- Glucagonoma - Glucagon-secreting tumor of the islet cells of the pancreas. Glucagon increases blood.
- Glucocortocoid deficiency - Decreased amount of hormone from the adrenal gland that increases.
- Glycogen-storage disease (Glycogenosis) - Any of a group of inherited disorders of glycogen.
- Glycogen - Substance formed from glucose, stored chiefly in the liver. When the blood-sugar level is.
- Goiter - Enlargement of the thyroid gland, which causes a swelling in the front part of the neck.
- Gonadal impairment - Decreased function of the gonads. See Gonads. Testes in men; ovaries in.
- Gonadal - Pertaining to gonads.
- Gonadotropin - Any hormone having a stimulating effect on the gonads.
- Gonads - Parts of the reproductive system that produce and release eggs (ovaries in the female) or.
- Gonorrhea - Infectious disease of the reproductive organs and other body structures that is sexually.
- Gout - Recurrent attacks of joint inflammation caused by deposits of uric acid crystals in the joints. It.
- Grand mal epilepsy - See Epilepsy, grand mal.
- Granulocytic leukemia - See Leukemia, granulocytic.
- Granulomas - Nodule of firm tissue formed as a reaction to chronic inflammation, such as from foreign.
- Granulomatosis - Formation of multiple granulomas. Each has nodules of granulated tissue forming a.
- Granulomatosus colitis - See Crohn's disease.
- Graves' disease - Disorder of the thyroid gland occurring most often in women. Characterized by.
- Growth hormone deficiency - Deficiency of hormone that results in dwarfism.
- Guillain-Barre syndrome - See Polyneuritis.
- HDL - High density liproprotein.
- Hageman factor (Factor XII) - Deficiency of this factor results in prolonged bleeding. See Factor.
- Hand-Schueller-Christian disease - Group of three symptoms that may occur in any of several.
- Hartnup disease - Hereditary disease that causes skin rash, unsteady gait and excess amino acids in.
- Hashimoto's thyroiditis - One of several kinds of thyroid gland inflammation.
- Heart attack - See Myocardial infarction.
- Heinz bodies - Granular deposits in red blood cells from precipitation of proteins. They are present in.
- Hemangioma - Benign tumor made up of a mass of blood vessels.
- Hematoma - Collection of blood that has escaped from a blood vessel and is localized in an organ or.
- Hematuria - Abnormal presence of blood in the urine. May be gross (can actually see the blood) or.
- Hemochromatosis - Disease in which excessive iron accumulates in the liver, pancreas and skin.
- Hemoconcentration - Decrease of the fluid content of the blood, with resulting increase in.
- Hemodilution - Increase in fluid content of blood, with resulting decrease in concentration of blood.
- Hemoglobin-C disease - Inherited blood disorder characterized by a moderate, chronic hemolytic.
- Hemoglobin-C trait - Relatively common abnormal hemoglobin in which lysine replaces glutamic acid.
- Hemolysis - Process by which red blood cells breakdown and hemoglobin is released. Occurs.
- Hemolytic anemia - See Anemia, hemolytic.
- Hemolytic disease - Disorder characterized by the premature destruction of red blood cells. May or.
- Hemolytic episode - Separation of hemoglobin from red blood cells.
- Hemolytic jaundice - Jaundice caused by severe hemolytic anemia, which results in high levels of.
- Hemolytic - Condition in which red blood cells break down and release the hemoglobin they contain.
- Hemophilia - Inherited deficiency of a blood clotting factor that may result in bleeding episodes.
- Hemophilus influenzae (haemophilus influenza, Type-B) - Bacteria that causes numerous diseases.
- Hemoptysis - Coughing up blood from the respiratory tract. Blood-streaked sputum can occur with.
- Hemorrhagic disease - Medical problem accompanied by uncontrolled bleeding. Hemorrhagic.
- Hemorrhagic gastritis - Inflammation of stomach accompanied by bleeding from stomach lining.
- Hemorrhoids - Dilated (varicose) veins of the rectum or anus. Usually caused by straining during bowel.
- Heparin therapy - Course of treatment with medication that prolongs blood clotting time. Used to.
- Heparinized - To render blood non-clottable with heparin. For example, tubes used to collect blood.
- Hepatic coma - Stupor or coma caused by waste products in the blood that are toxic to the brain.
- Hepatic disease - Any disease involving the liver, including many types of hepatitis and cirrhosis.
- Hepatic dysfunction - Poor liver function.
- Hepatic - Of or affecting the liver.
- Hepatitis profile - Cost is about $18.00. Blood tests performed include hepatitis-B surface antigen.
- Hepatitis-B - Form of viral hepatitis caused by the hepatitis-B virus. Characterized by rapid onset of.
- Hepatitis - Inflammatory liver condition characterized by jaundice, enlarged liver, loss of appetite.
- Hepatocellular injury - Injury of liver cells.
- Hepatomas (Malignant liver tumor; hepatocellular carcinoma) - Malignant tumor that begins in.
- Hepatotoxicity - Tendency of a substance, usually a medication or alcohol, to have a destructive effect.
- Hereditary anti-edema - Inherited condition that prevents accumulation of fluid.
- Hereditary spherocytosis - Inherited disorder characterized by small, spherical red blood cells.
- Hereditary - Transmitted genetically from generation to generation.
- Hernia - Protrusion of an internal organ through a weakness or abnormal opening in the muscle around.
- Herpes - Herpes type-1 causes common cold sores, which appear around the mouth. Herpes type-2.
- Hgb-C disease (Hemoglobin-C disease) - See Hemoglobin-C trait.
- Hiatal hernia - Abnormal weakness or opening in the diaphragm. Allows a portion of the stomach to.
- High-purine diet - Diet of foods that are high in purines, including anchovies and sardines, organ.
- Histidinemia - Hereditary defect of metabolism marked by excess histidine (an amino acid) in the.
- Histology - Science dealing with the microscopic identification of cells and tissue.
- Histoplasmosis - Fungal infection from breathing dust that contains fungus spores or through direct.
- Hodgkin's disease - Malignant tumor of the lymph glands characterized by progressive enlargement of.
- Hodgkin's lymphoma - See Hodgkin's disease.
- Homocystinuria - Rare, hereditary defect of metabolism, marked by excess homocystine (an amino.
- Humoral - Relating to any fluid or semifluid of the body.
- Huntington's chorea - Rare, abnormal, hereditary condition characterized by involuntary, purposeless.
- Hydatidiform mole - Disease occurring during early pregnancy resulting in death of the fetus and an.
- Hydrocephalus - Condition characterized by an excessive accumulation of fluid with the cranial vault.
- Hydronephrosis - Caused by an obstruction in the tube that carries urine from the kidney to the.
- Hyper - Abnormally increased; excessive.
- Hyperalimentation - Supplying total nutritional needs of patients who are unable to eat normally by.
- Hypercalcemia - Presence of excessive calcium in the blood. May result from tumor of the parathyroid.
- Hyperchloremia - Presence of excessive amounts of chloride in the blood. May result from severe.
- Hyperfibrinogenemia - Presence of excessive fibrinogen in the blood. See Fibrinogen. May indicate.
- Hyperfunctioning tumor - Any tumor that leads to higher than normal action of the chemicals (usually.
- Hyperinsulinism - Excessive secretion of insulin.
- Hyperkalemia - Abnormally high blood potassium level. May be seen in people who have suffered.
- Hyperlipoprotenemia - Condition in which excessive lipoproteins (cholesterol and other fatty.
- Hypermagnesemia - Elevated levels of magnesium in the blood. Most commonly occurs in people.
- Hypernatremia - Excess of sodium in the blood, usually caused by excessive loss of water and.
- Hyperoxaluria - Hereditary defect of metabolism, marked by excessive oxalate in the urine. May result.
- Hyperparathyroidism - Excessive amounts of parathyroid hormone circulating in the blood. Excess.
- Hyperphosphatemia - Abnormally high level of phosphates in the blood. May result from bone.
- Hyperploidy - Condition of having one or more chromosomes in excess of the normal number. The.
- Hyperprolinemia, Type-A - Disorder of amino acid metabolism.
- Hypertension (High blood pressure) - Increase in the force of blood against the arteries as blood.
- Hyperthyroidism - Overactivity of the thyroid, an endocrine gland that regulates all body functions.
- Hypertonic - Solution that contains substances that flow outward through a semipermeable membrane.
- Hypertrophic anal papilla - Excessive growth of the papilla of the rectum. See Papilla.
- Hypertrophic cardiomyopathy - See Cardiomyopathy.
- Hypertrophy - Increase in the size of a cell or group of cells. Causes an increase in the size of an organ.
- Hyperventilation - Breathing so rapidly that carbon dioxide levels in the blood are decreased.
- Hypo - Deficient; beneath; under.
- Hypoalbuminemia - Abnormally low levels of albumin (protein) in the blood.
- Hypoalderostonism - Deficiency of aldosterone secreted by the outer layer of the adrenal glands. May.
- Hypocalcemia - Abnormally low level of calcium in the blood. May result from hypoparathyroidism or.
- Hypochloremia - Abnormally low levels of chloride in the blood. Low chloride levels can occur from.
- Hypochromic anemia - See Anemia, hypochromic.
- Hypofibrinogenemia - Abnormally decreased level of fibrinogen in the blood. See Fibrinogen. May.
- Hypofunctioning tumor - Tumor that causes the anatomical part it encroaches on to have less than.
- Hypogammaglobulinemia - Abnormally low levels of gammaglobulins in the blood, which results in an.
- Hypoglycemia - Abnormally low blood sugar level caused by abnormal function, not disease, of the.
- Hypoglycemic syndrome - Condition caused by low blood sugar, characterized by cold sweat, low.
- Hypogonadism - Decreased functional activity of gonads, with hindered growth and slowed sexual.
- Hypogonadotropism - Abnormal condition caused by decreased production of gonadotropins. See.
- Hypokalemia - Below normal level of potassium in the blood. May result from aldosteronism.
- Hypolipoproteinemia - Abnormally low levels of lipoproteins in blood.
- Hyponatremia - Less than normal concentration of sodium in the blood. Caused by excessive water in.
- Hypooxaluria - Decreased amount of oxalic acid in the urine.
- Hypoparathyroidism - Decreased production of hormones by the parathyroid glands, causing low.
- Hypophosphatasia - Inborn error of metabolism that causes difficulty building and healing bones.
- Hypophysectomy - Surgical removal of the pituitary gland.
- Hypopituitarism - Underactivity of the pituitary gland, resulting in inadequate hormone production.
- Hypoplasia - Incomplete development or underdevelopment of an organ or tissue, usually from a.
- Hypoplastic anemia - See Anemia, hypoplastic.
- Hypotension - Abnormally low blood pressure. One symptom of shock.
- Hypothyroidism, primary - Caused by dysfunction of the thyroid gland and may be due to surgical.
- Hypothyroidism, secondary - Caused outside the thyroid. It may result from decreased activity of the.
- Hypothyroidism - Underactive thyroid gland, which results in decreased metabolic rate. Early.
- I.V. - See Intravenously.
- Ichthyosis - Skin condition in which skin is dry, thickened and fissured, resembling fish scales. Usually.
- Ichythosis follicularis - Skin disorder characterized by dryness, roughness and scaliness.
- Idiopathic cold-agglutinin diseases - Disease of unknown cause associated with laboratory findings.
- Idiopathic hypertrophic subaortic stenosis (IHSS) - Chronic heart condition that produces an.
- Idiopathic thrombocytopenic purpura (ITP) - Bleeding into the skin and other organs due to a.
- Idiopathic-acquired hemolytic anemia - See Anemia, idiopathic-acquired hemolytic.
- Idiopathic - Without known cause.
- Ileitis - See Crohn's disease.
- Immune - Resistance or protection against infection by the body's natural defenses. A person may be.
- Immunodeficiency diseases - Defects in the body's immune system. A healthy immune system.
- Immunoglobin-deficiency disease - Illness caused by deficiency of a protein molecule with known.
- Immunomedicated disease - Illness caused by medicines that decrease the efficiency of the immune.
- Immunosuppressive therapy - Drugs used to prevent the body from forming a normal immune.
- Immunotherapy - See Immunosuppressive therapy.
- Infarction - Tissue death due to the obstruction of blood to that tissue.
- Infectious mononucleosis - Infectious viral disease that affects the liver, respiratory system and.
- Inferior vena cava - Large vein that returns unoxygenated blood to the heart from parts of the body.
- Inflammatory bowel disease - Characterized by fever, pain, abscess formation, severe diarrhea.
- Influenza - Common, contagious respiratory infection caused by a virus. Incubation after exposure is.
- Insulin-resistant states - Severe insulin dependent diabetes mellitus that no longer responds to.
- Insulinoma - Benign (nonmalignant) tumor of insulin secreting cells of the islets of Langerhans in the.
- Intermittent positive-pressure-breathing therapy - Form of treatment for disorders of the lungs.
- Interstitial fibrosis - Formation of fibrous tissue between normal tissues.
- Interstitial - Occupies space between tissues, such as interstitial fluid.
- Intestinal fistula - Abnormal opening leading from the intestinal tract to another abdominal organ or to.
- Intraepithelial neoplasia - Small tumor or cancer in the epithelial layer of the skin.
- Intravenously (I.V.) - Through a vein.
- Intrinsic factor levels - Substance secreted by the stomach lining that is necessary for vitamin B-12 to.
- Iodine-deficient goiter - Enlarged thyroid gland due to too little iodine in the diet. Iodine is an essential.
- Iritis - Inflammation of tissues that support the iris (the ring of colored tissue around the pupil of the.
- Iron overload - Too much iron in blood, liver or other organs.
- Iron-deficiency anemia - See Anemia, iron deficiency.
- Ischemia - Decreased blood supply to a body organ or part.
- Ischemic bowel disease - Intestinal problems caused by inadequate supply of blood to the cells of the.
- Ischemic - Condition in which there is decreased blood flow to a body organ or part.
- Isichromosome - Abnormal chromosome characterized by abnormal splitting of a chromosome during.
- Isoenzyme - One of many forms of a protein catalyst differing in characteristics (chemical, physical.
- Isothermal infusion - Injection with a fluid at the same temperature as the recipient.
- Jaeger card - Card with printed letters of varying sizes. Used to test vision.
- Jaundice - Condition of yellow skin, yellow whites of the eyes, dark urine and light-colored stools. It is.
- Karotyping - Determining the chromosome constitution of the nucleus of a cell. Useful in predicting.
- Keloids (Cheloids) - Overgrowth of scar tissue at the site of a wound on the skin. New scar tissue is.
- Keratosis follicularis - Uncommon hereditary skin disorder characterized by small, horny growths that.
- Keratosis - Any horny growth, such as a wart.
- Ketoacidosis - Serious disorder that results from a deficiency or inadequate use of carbohydrates.
- Ketone bodies - Substances formed when the body rapidly breaks down fats to use for energy.
- Ketonuria - Presence of ketone bodies in the urine. Usually seen in people with uncontrolled diabetes.
- Kidney shut down (Kidney failure; renal failure) - Sudden failure of kidneys to function. Usually.
- Kidney stones - Hard, unyielding material produced by the kidney. May lodge in the kidney or pass.
- Klippel-Feil syndrome (Congenital short-neck syndrome) - Rare, congenital malformation of the.
- Kyphosis - Abnormal condition in which the upper spinal column (between the neck and midback).
- L/S ratio - Ratio of lecithin to sphingomyelin. Abnormalities may represent the possibility of an.
- LDL - Low density lipoprotein.
- Lactic acidosis - Increased acidity in body due to accumulation of excessive lactic acid production.
- Laennec's cirrhosis - Cirrhosis of the liver associated with alcohol abuse. See Cirrhosis.
- Laryngospasm - Spasmotic closure of the larynx or voice box. When spasms occur, air cannot pass.
- Larynx - Part of the air passage connecting the throat with the trachea or windpipe.
- Lateral sclerosis - Degeneration of the lateral columns of the spinal cord.
- Leprosy - Chronic disease characterized by the production of fibrous connective-tissue lesions.
- Lesion - Injury or damage to an organ or tissue.
- Leukemia, acute - Malignant overgrowth of white blood cells in bone marrow or tissues that are part.
- Leukemia, granulocytic - Malignant blood disease of granulocytes, a form of white blood cell.
- Leukemia, lymphatic - Cancer that primarily involves lymphatic cells. Affects children and adults.
- Leukemia, lymphocytic - Very slow-growing cancer of blood-forming organs in older people. About.
- Leukemia, monocytic - Malignancy of blood-forming tissues in which the predominant cells are.
- Leukemia, myeloblastic - Malignancy of blood cells in which the predominant cells are myeloblasts (a.
- Leukemia, myelogenous - See Leukemia, myelocytic.
- Leukemia, myeloid - Malignancy of white blood cells with polymorphonuclear cells predominant.
- Leukemia, myelomonocytic - Malignancy of blood cells in which the predominant cells are.
- Leukemia, myleocytic - Disorder characterized by the unregulated, excessive production of.
- Leukoagglutinins - Antibodies directed against white blood cells.
- Liothyronine (T3 3) toxicosis - Overactive thyroid function due to T3 poisoning.
- Liver profile - Cost is about $20.00. Blood tests performed include Bilirubin, Protein, LDL, Alkaline.
- Lordosis - Forward curvature of the lumbar spine (the small of the back).
- Lumbar stenosis - Narrowing or stricture in the lower part of the back.
- Lupus erythematosus, systemic - Inflammatory disease of connective tissue. Symptoms may include.
- Luteinization - Process by which a follicle in the ovary transforms into a luteum.
- Luteinized granulosa - Thick, scarred, yellow lesion.
- Luteum - Yellow-colored cyst.
- Lymph - Transparent, slightly yellow liquid found in lymph vessels throughout the body. Derived from.
- Lymphatic leukemia - See Leukemia, lymphatic.
- Lymphatic system - Vast, complex network of vessels, valves, ducts, nodes and organs that help.
- Lymphatic - Pertaining to lymph system of the body.
- Lymphoblastic lymphoma (Lymphoblastoma; lymphoblastic lymphosarcoma) - Malignant tumor.
- Lymphocyte - One of several types of white blood cell that help fight infection.
- Lymphocytic leukemia - See Leukemia, lymphocytic.
- Lymphocytic proliferative disease - Disease with an overproduction of lymphocytes, one form of.
- Lymphoma - Disorders involving new, abnormal growth or tumor of lymph tissue. Usually malignant.
- Lymphoreticular malignancy - Cancer of the reticuloendothelial cells of lymph nodes. See.
- Lymphosarcoma - Malignant tumor of the lymph glands. More common than Hodgkin's disease. See.
- Lysis - Destruction or breakdown, as of a cell or other substance.
- Macroamylaemia - Excess of starch in the blood.
- Macrocytic anemia - See Anemia, macrocytic.
- Macroglobulinemia - See Waldenstrom's macroglobulinemia.
- Macular disease - Stain, spot or thickening of the cornea.
- Malabsorption syndromes - Poor absorption of nutrients from the intestinal tract into the blood.
- Malaise - Vague feeling of body discomfort.
- Malaria - Infection caused by a single cell parasite transmitted by the bite of an anopheles mosquito.
- Male menopause - Symptoms, such as depression, change in libido, impotence, in men at midlife.
- Malignant - Capable of causing destruction of normal tissue; may lead to death. Usually refers to.
- Mallory-Weiss syndrome - Condition characterized by massive bleeding following a tear in the.
- Maple-syrup urine disease - Hereditary defect of metabolism. Usually diagnosed in infancy because.
- Mast cells - Part of connective tissue.
- Mastocytosis - Overproduction of mast cells. May rarely infiltrate liver, spleen, bones, the.
- Mean corpuscular hemoglobin (MCH) - See Red cell indices.
- Mean corpuscular hemoglobin concentration (MCHC) - See Red cell indices.
- Meconium ileus - Obstruction of the small intestine in the newborn caused by a plug of meconium. See.
- Meconium - Thick, sticky, dark-green material that collects in the intestines of a fetus and forms the.
- Mediastinitis - Inflammation of the mediastinum. See Mediastinum.
- Mediastinum - Central portion of the chest cavity that contains the heart and its large blood vessels.
- Medulla - Most internal part of a structure or organ.
- Medullary - See Medulla.
- Megaloblastic anemia - See Anemia, megaloblastic.
- Melanin - Dark pigment of the skin, hair and iris of the eye.
- Melanocytes - Cells that produce melanin.
- Melanoma - Any of a group of malignant tumors, primarily of the skin, made up of melanocytes. See.
- Meninges - Thin membranes that cover the brain and spinal cord.
- Meningioma - Hard, usually vascular tumor of the membranes covering the brain and spinal cord.
- Meningitis - Inflammation or infection of the meninges. See Meninges. It is contagious and may be.
- Meningocele (Meningoencephalocele) - Hernia protrusion of the brain and its coverings through a.
- Menke's kinky-hair syndrome - Inherited disorder caused by a defect in intestinal absorption of.
- Menopause - Permanent cessation of menstruation. Occurs as early as age 35 or as late as age 55;.
- Menstrual - Pertaining to menstruation. See Menstruating.
- Menstruating - Normal discharge of blood and tissues through the vagina that come from the uterine.
- Mesenteric adenitis - Lymph glands in mesentery become inflamed. Symptoms may mimic.
- Mesentery - Membranous folds that hold and suspend the small intestines.
- Metabolic alkalosis - Too much base in the body due to loss of acid.
- Metabolism - Sum of all the chemical and physical processes by which living substance is produced.
- Metabolites - Any substance produced by metabolism. See Metabolism.
- Metachromatic leukodystrophy - Inherited condition that causes blindness, mental retardation.
- Metamorphopsia - Defective vision in which objects appear distorted. Sometimes results from disease.
- Metastasis - Process by which cancerous cells or infectious germs spread from their original location.
- Metastatic cancer - Cancerous cells that spread from their original location to other parts of the body.
- Metastatic disease - Disease that has transferred from an organ or body part not directly connected.
- Metastatic - Pertaining to metastasis. See Metastasis.
- Microaneurysms - Microscopic aneurysms, characteristic of certain diseases. Capillary.
- Microbes - Microorganism (small, living organism) capable of producing disease.
- Microcytic anemia - See Anemia, microcytic.
- Miliary tuberculosis - Acute infection associated with the spread of tuberculosis throughout the body.
- Mitogen - Substance that triggers mitosis. See Mitosis.
- Mitosis - Type of cell division in which the body produces new cells for growth and repair of injured.
- Mitral regurgitation - Defective closure of the heart's mitral valve, which allows some of the blood to.
- Mitral stenosis - Calcification and decreased function of the heart's mitral valves.
- Mitral valve prolapse - Condition in which the mitral valve becomes FLOPPY, resulting in mitral.
- Mitral valve - Valves located in the heart between the left atrium and left ventricle.
- Mixed connective tissue disease (MCTD) - Disease affecting the entire body characterized by the.
- Monocytic leukemia - See Leukemia, monocytic.
- Mononucleosis - See Infectious mononucleosis.
- Monosomy - Chromosomal abnormality characterized by the absence of one chromosome from the.
- Motility disorders - Any disorder or disease characterized by inability to remove intestinal waste.
- Mucocele - Dilation of a cavity with accumulated mucus secretion.
- Mucopolysaccharides - Chemicals that contain hexosamine combined with proteins.
- Mucopolysaccharidosis - Any of a group of genetic disorders caused by a defect in metabolism of.
- Multinodular goiter - Enlarged thyroid gland causing a swelling in the front part of the neck. See.
- Multiple myeloma (Primary bone marrow cancer) - Malignancy beginning in the plasma cells of the.
- Multiple sclerosis (MS) - Chronic disorder affecting many nervous system functions. Patches of white.
- Mumps - Mild, contagious, viral disease that causes painful swelling of the salivary glands. Other.
- Muscular dystrophy - Gradual deterioration of the muscles of the body, leading to increasing difficulty.
- Myasthenia gravis - Disorder of muscles, especially the face and head, with increasing fatigue and.
- Mycoplasma pneumonia - Lung infection caused by germ mycoplasma.
- Myeloblastic leukemia - See Leukemia, myeloblastic.
- Myelocele - Saclike protrusion of the spinal cord through a congenital defect in the spinal column.
- Myelocytes - Immature white blood cells normally found in bone marrow.
- Myelocytic leukemia - See Leukemia, myelocytic.
- Myelogenous leukemia - See Leukemia, myelocytic.
- Myeloid leukemia - See Leukemia, myeloid.
- Myelomonocytic leukemia - See Leukemia, myelomonocytic.
- Myelosuppressive - Inhibiting bone marrow activity, resulting in the decreased production of blood.
- Myocardial failure - Condition that exists when the heart is no longer able to pump all the blood.
- Myocardial fibrosis - Formation of fibrous material in the heart.
- Myocardial infarction (Heart attack) - Death of heart muscle cells from reduced or obstructed.
- Myocarditis bacterial - Inflammation of heart muscle (myocardium) caused by bacterial infection.
- Myocarditis - Inflammation of the heart muscle (myocardium) that usually occurs as a complication of.
- Myocardium - Heart muscle.
- Myoglobin - Chemical stored in muscle that contains iron and oxygen.
- Myxedema - Condition of swollen lips, thickened nose, swelling of the skin and mental dullness caused.
- Necrosis - Localized death of tissue that occurs in groups of cells in response to disease or injury.
- Neisseria meningitides - Bacteria that is often the cause of meningitis. See Meningitis.
- Neoplasms - Any abnormal growth of new tissue.
- Neoplastic diseases - Disease characterized by abnormal growth of new tissue. Cell multiplication is.
- Nephritis - Any one of a large group of diseases of the kidney characterized by inflammation and.
- Nephron - Anatomical and functional unit of the kidney consisting of tubules and blood vessels.
- Nephrosclerosis (Nephroangiosclerosis) - Involves small arteries and kidney's filtering system.
- Nephrosis (Nephrotic syndrome) - Form of chronic kidney disease beginning in early childhood.
- Nephrostomy tube - Flexible plastic tube passed into an opening made in the kidney that leads outside.
- Nephrotic syndrome - See Nephrosis.
- Neurinoma - Tumor of the nerve covering. Usually benign, but may undergo malignant change.
- Neuritis - Inflammation of a nerve. Can cause pain, numbness, paralysis or sensitivity of the affected.
- Neuroblastoma - Highly malignant tumor that usually originates in the adrenal glands of young children.
- Neurofibroma - Fibrous tumor of nerve tissue.
- Neurogenic - 1) Forming nervous tissue or stimulating nervous energy. 2) Originating in the nervous.
- Non-Hodgkin's lymphoma (Lymphosarcoma) - Malignant tumor of the lymph glands, which is more.
- Non-specific liver disease - Poor liver function in the absence of a known cause.
- Non-spherocytic hemolytic anemia - See Anemia, non-spherocytic hemolytic.
- Nystagmus - Involuntary, rapid movements of the eyeball. Usually caused by an underlying disease.
- Obstructive jaundice (Cholestasis) - Interruption in the flow of bile through any part of the biliary.
- Occlusion - Closing or obstruction. Usually describes a blockage in blood vessels.
- Occult - Hidden from view; difficult to observe directly.
- Opacified - Impervious to light rays or X-rays.
- Optic atrophy - Degeneration of the optic nerve.
- Optic neuritis - Inflammation of the nerve that conducts vision impulses from the eye to the brain.
- Osteoarthritis (Degenerative joint disease) - Degeneration of cartilage at a joint and growth of.
- Osteochondritis dissecans - Inflammation of bone and cartilage, which results in pieces of cartilage.
- Osteochondromas - Benign tumors made of bone and cartilage.
- Osteochondromatosis - Occurrence of multiple osteochondromas. See Osteochondromas.
- Osteomalacia - Abnormal condition resulting in softening of bone. Accompanied by weakness.
- Osteomyelitis - Infection of the bone and bone marrow caused by bacteria, usually staphylococcus.
- Osteoporosis - Loss of normal bone density, mass and strength, leading to increased porousness and.
- Ovarian agenesis - Congenital absence of ovaries resulting in sterility.
- Overhydration - Too much fluid in tissues.
- Peptic ulcer - Lesion of the mucous membrane lining of the stomach, duodenum or of any part of the.
- Percutaneous - Performed through the skin. In some procedures, a needle is passed through the skin.
- Pericardial effusion - Escape of fluid. into the pericardium. See Pericardium.
- Pericarditis, acute - Inflammation of the sac that covers the heart. Symptoms may include chest pain.
- Pericardium - Thin, membranous, double-layered covering of the heart.
- Periodontal disease (Periodonitis) - Inflammation and infection of the gums, causing loss of.
- Peripheral circulation (Peripheral vascular system) - Network of arteries, veins and lymphatic.
- Peripheral vessels - See Peripheral circulation.
- Peripheral-artery disease - Any abnormal condition that affects the arteries outside the heart. Signs.
- Peritoneum - Covering of the intestinal tract and lining of the walls of the abdominal and pelvic cavities.
- Peritonitis - Serious infection or inflammation of part or all of the peritoneum. May be fatal if not.
- Pernicious anemia - See Anemia, pernicious.
- Petechiae - Tiny purple or red spots that appear on the skin as a result of very minute hemorrhages.
- Petit mal epilepsy - See Epilepsy, petit mal.
- Pharyngeal - Pertaining to the pharynx or voice box in the throat, which contains the vocal cords.
- Pharyngitis - Throat inflammation and infection that can be caused by a variety of germs (bacteria.
- Phenylketonuria (PKU) - Inherited disorder marked by the inability of phenylalanine (an amino acid).
- Pheochromocytoma - Tumor of the core (medulla) of the adrenal glands. Tumor is usually benign and.
- Phlebitis - Inflammation of a vein.
- Phototherapy - Treatment of a disease by exposure to light, especially variously concentrated light.
- Pituitary diabetes insipidus - Metabolic disorder due to injury of the pituitary gland causing a.
- Placenta previa - Bleeding late in pregnancy caused by placenta attaching too low in the uterus.
- Placental sulfatase deficiency - Deficiency of sulfatase in the placenta.
- Plaques - 1) Small raised area of abnormal material on a surface, such as the skin or blood vessel.
- Plasma - Fluid part of the blood after blood cells and other particles are removed.
- Plasmapheresis (Therapeutic plasma exchange; TPE) - Blood is withdrawn from a vein in the arm.
- Plasmin - Active portion of the chemical system that causes blood clots to dissolve.
- Plasminogen-activator system - System that stimulates the conversion of chemical substances to.
- Platelets - Tiny blood cells (much smaller than red or white blood cells) that assist in blood clotting. A.
- Pleura - Thin tissue lining of the lungs and chest cavity.
- Pleural - Relating or pertaining to pleura. See Pleura.
- Pleurisy - Inflammation of the pleura. See Pleura. A painful condition caused by lung disease.
- Pneumatosis cytoides intestinalis - Disease characterized by the presence of air or gas in abnormal.
- Pneumonia - Inflammation of the lung(s) resulting in tiny air sacs in the lung becoming plugged with.
- Pneumonitis - Inflammation of lung tissue that may be caused by a virus or it may be an allergic.
- Pneumothorax - Collapse of all or part of a lung caused by pressure from free air in the chest between.
- Polycystic ovaries (Stein-Leventhal syndrome) - Ovary enlargement from many small cysts. Ovary.
- Polycystic - Containing many cysts.
- Polycythemia vera - Overproduction of red blood cells, white blood cells and platelets. Cause is.
- Polycythemia - Increase in red blood cells in the body. The disease has three forms. Polycythemia vera.
- Polymyositis - Inflammation of many muscles at one time. Usually accompanied by muscle weakness.
- Polyneuritis - Inflammation of many nerves simultaneously. In acute infectious polyneuritis.
- Polyposis - Formation of numerous polyps. See Polyps. Familial polyposis is an inherited condition in.
- Polyps - Growths. Often on a stalk arising from dry mucous membranes, such as in the nose, cervix or.
- Porphyria cutanea tarda - Type of porphyria usually associated with chronic alcoholism marked by.
- Porphyria, acute intermittent (AIP) - Rare inherited disorder characterized by excessive formation.
- Porphyria - Excretion of porphyrins into the urine. See Porphyrins.
- Porphyrins - Any of a group of pyrrole derivatives found in cytoplasm. These combine with iron and.
- Portacaval shunt - Connection of the portal vein with the vena cava to release backed-up pressure in.
- Portal hypertension - Higher than normal blood pressure in the large vein that collects nourishment.
- Post-streptococcal glomerulonephritis - Inflammatory disease of kidney occurring about 3 weeks.
- Pott's disease (Tuberculous spondylitis) - Rare, grave form of tuberculosis that is located in the.
- Pre-eclampsia (Toxemia of pregnancy) - Serious disturbance in blood pressure, kidney function and.
- Precocious puberty - Changes of adolescence that occur sooner than expected in young girls or boys.
- Primary biliary cirrhosis - Disease of the liver caused from chronic bile retention. Cause is unknown.
- Primary hypothyroidism - Overabundance of aldosterone, a hormone produced and secreted by the.
- Primary lymphedema - Chronic swelling of a part due to the accumulation of fluid (lymph) caused by.
- Proctitis - Inflammation of the rectum and tissues around the anus. Can be caused by sexually.
- Profile - Most hospital and commercial laboratories offer blood tests collected together in.
- Prolonged activiated partial thromboplastin time - Longer-than-normal time required for clotting to.
- Prostate - Gland surrounding the neck of the bladder and urethra in men.
- Prostatic hypertrophy - Enlargement of the prostate. See Prostate. May obstruct the flow of urine.
- Prostatitis - Inflammation or infection of the prostate. See Prostate. Not contagious. Symptoms may.
- Protein metabolism - Process by which protein foods are used by the body to make tissue proteins.
- Proteus infections - Bacteria normally found in feces, water and soil. May cause urinary tract.
- Pseudo-precocious puberty - Premature sexual development; of unknown cause.
- Pseudocysts - Abnormal or dilated space resembling a cyst but without a membrane lining. Condition.
- Pseudogout - Arthritic condition marked by attacks of gout-like symptoms, usually affecting a single.
- Pseudohypoparathyroidism - Hereditary condition that resembles hypoparathyroidism. In.
- Pseudomembranous enterocolitis (Necrotizing enterocolitis) - Acute inflammatory bowel disorder.
- Pseudotumors - False or phantom tumor.
- Psoriasis - Chronic, scaly skin disorder characterized by frequent remissions and recurrences. Affected.
- Pulmonary disease - Lung disease.
- Pulmonary edema - Accumulation of fluid in the lungs. Caused by a failing heart.
- Pulmonary embolism - Blood clot or fat cells (rarely) in one of the arteries carrying blood to the lungs.
- Pulmonary fibrosis - Fibrous tissue in the lungs causing scarring of tissue from one of many disease.
- Pulmonary infarctions - Death of a section of lung tissue from obstruction of the blood supply. See.
- Pulmonary insufficiency - Subnormal function of the lungs.
- Pulmonary valve - Separates the right bottom chamber of the heart (ventricle) from the pulmonary.
- Pulmonary-valve stenosis - Narrowing of the pulmonary valve. Impairs heart function. Usually there.
- Pulmonary - Lungs.
- Purines - Any of a large group of nitrogen compounds. End products after digestion of certain proteins;.
- Purpura - Purplish or brownish discoloration easily seen through the skin caused by bleeding into the.
- Pyelonephritis (Kidney infection) - Noncontagious bacterial infection of the kidneys. Infection may.
- Pyloric stenosis - Condition in infancy in which encircling muscles enlarge and cause obstruction. It.
- Pyridoxine-responsive anemia - See Anemia, pyridoxine-responsive.
- Radiation therapy (Radiotherapy) - Use of high-energy waves, generated by special X-ray.
- Radiography - Making X-ray films of internal structures of the body by exposure of film specially.
- Radioisotope scan - Radioisotope is given orally or intravenously and becomes concentrated in.
- Radioisotope - Radioactive form of chemical normally present in the body. Chemical elements that give.
- Radiotherapy - See Radiation therapy.
- Raynaud's disease - Primary disorder of the circulatory system that affects blood circulation to fingers.
- Raynaud's phenomenon - Circulation system disorder affecting fingers and toes. A complication of an.
- Rebound stimulation - Response is reversed when stimulus is withdrawn.
- Red cell indices - Blood test that provides important information about the size, hemoglobin.
- Red measles (Rubeola) - Serious viral disease of childhood. Uncommon today because.
- Reflux esophagitis - Irritation of the esophagus from stomach acid splashing upward into the.
- Reiter's disease - Inflammatory disease caused by symptoms resembling those of arthritis, urethritis.
- Renal disease - Any of several diseases affecting the kidneys.
- Renal plasma flow - Rate of blood flow through the kidney.
- Renal tubular acidosis - Loss of base or accumulation of acid in the body due to disease of the.
- Renal tubular disease - Disease of the kidney tubules.
- Renal - Pertaining to the kidney.
- Renovascular hypertension (Portal hypertension) - Abnormally high blood pressure within the.
- Restrictive pericarditis - Pressure develops when an increasing amount of fluid restricts the pumping.
- Reticulocytes - Young, immature red blood cells.
- Reticulocytosis - Excess amount of reticulocytes in the blood.
- Reticuloendothelial system - Body system involved primarily in defense against infection and in.
- Retina - Innermost part of the eyeball.
- Retinitis pigmentosa - Hereditary disease marked by progressive loss of retinal response, leading to.
- Retinopathy - Any non-inflammatory disease of the retina. Associated with various conditions. It is.
- Retroperitoneal thrombosis - Clotting of blood in the retroperitoneal space.
- Retroperitoneal - Pertaining to organs closely attached to the abdominal wall, behind the peritoneum.
- Reye's syndrome - Disease in children and adolescents that involves brain and other major organs.
- Rh-factor - Symbol for rhesus factor. Antigens present on the surface of red blood cells.
- Rh-isoimmunization - Development of agglutination against Rh-blood group antigens in an Rh-negative.
- Rheumatic fever - Inflammatory complication of Group-A strepococcal infections that affects many.
- Rheumatoid arthritis - Illness characterized by joint disease that involves muscles, cartilage and.
- Rickets - Condition caused by insufficient intake or absorption of vitamin D coupled with too little.
- Rickettsial disease - Any disease caused by rickettsial microorganisms. Transmitted to humans by.
- Rickettsial germs - Microorganisms smaller than bacteria and larger than viruses. Cause various.
- Rickettsial-collagen disease - Connective tissue disease caused by rickettsial germs.
- Ring-chromosome formation - Chromosome in which both ends have been lost; broken ends have.
- Rocky Mountain spotted fever - Caused by rickettsial germs transmitted by a tick bite. Symptoms.
- Rubella (German measles) - Mild, contagious viral illness. Likely to cause serious birth defects to an.
- Salivary-gland disease - Disease of the salivary glands, which secrete saliva.
- Salmonella - Thousands of kinds of salmonella bacteria cause many diseases, including typhoid fever.
- Salt-losing syndrome - Condition characterized by vomiting, dehydration, abnormally low blood.
- Sandhoff's disease - Variant of Tay-Sachs disease that has a progressive, more rapid course. Found.
- Sarcoidosis - Chronic, progressive disease of unknown cause. May cause symptoms in the skin, lungs.
- Sarcoma - Tumor derived from connective tissue.
- Scan - Shortened form of scintiscan, a diagnostic procedure using a scintillation camera to record.
- Scarlatina (Scarlet fever) - Childhood disorder characterized by a bright-red rash. Scarlet fever is.
- Scarlet fever - See Scarlatina.
- Scleroderma - Widespread connective tissue disease in which skin and other body parts gradually.
- Sclerosing cholangitis - Scarring and inflammation of a bile duct.
- Scoliosis - Abnormal lateral curve of a normally straight spine.
- Scotoma - Area of depressed or decreased vision in the visual field that is surrounded by an area of.
- Scurvy (Vitamin-C deficiency) - Illness caused by inadequate intake of vitamin C. Vitamin C is.
- Seborrheic dermatitis - Skin condition characterized by greasy or dry, white scales. Dandruff and.
- Secondary hypothyroidism - Low thyroid function from drugs or other cause.
- Secondary lymphedema - Swelling of a body part due to the accumulation of fluid caused by.
- Secondary syphilis - Second stage of syphilis, characterized by skin rash, fever, swollen glands and.
- Sella turcica - Depression in the floor of the skull that contains the pituitary gland.
- Sensorineuraly deafness - Loss of hearing due to a lesion in the acoustic nerve (the eighth cranial.
- Septal defects - Abnormal, usually congenital, defect in the wall separating two chambers of the heart.
- Septic arthritis - Infection in any joint in the body. See Arthritis.
- Serous - Pertaining to or resembling serum. See Serum.
- Serum sickness - Hypersensitivity reaction following administration of an antiserum. Characterized by.
- Serum - Liquid portion of the blood that remains after blood cells have been removed.
- Sexual precocity - Attainment of sexual maturity before the 6th birthday in girls and the 8th birthday in.
- Shigellosis - Dysentery produced by an infection by a shigella germ.
- Sickle cell anemia - See Anemia, sickle cell.
- Sickle cell trait - Anemia and other signs of sickle cell anemia do not occur in the person with sickle.
- Sigmoid torsion - Twisting of the sigmoid portion of the large intestine.
- Sigmoid - Portion of the large intestine located in the left side of the abdomen. It connects to the.
- Single-vessel disease - Disease involving only one of the coronary artery vessels. See Coronary.
- Sinusitis - Inflammation or infection of the sinuses. Usually refers to the eight sinuses adjacent to the.
- Sjogren's disease - See Sjogren's syndrome.
- Sjogren's syndrome - Benign, chronic inflammation that results in diminished production of tears and.
- Snellen chart - One of several charts used to test vision. Letters, numbers or symbols are arranged on.
- Solid tumors - Growth of tissue of hard, unyielding substance. Differs from a tumor filled with fluid.
- Specificity - Quality or state of being specific. Usually refers to restriction of effect to a particular.
- Spherocytes - Abnormally shaped red blood cells. Cells are sphere shape, in contrast to the doughnut.
- Spherocytosis - Presence of spherocytes in the blood. Caused by some anemias. See Anemia.
- Sphincter of Oddi - Sphincter muscle of the bile duct.
- Spina bifida - Inherited defective closure of the body encasement of the spinal cord through which the.
- Spleen - Large organ on the left side of the upper abdominal cavity next to the stomach. Helps modify.
- Splenectomy (Spleen removal) - Removal of the spleen due to injury (causing rupture and.
- Spondylolisthesis - Forward displacement of one vertebra upon another, usually the fifth lumbar over.
- Sprue - Chronic disorder resulting from malabsorption of nutrients from the small intestine. It occurs in.
- Staphylococcemia - Infection caused by staphylococcus bacteria in the blood. May result in.
- Staphylococcus aureus - Bacteria that frequently causes diseases of the skin and other organs.
- Steatorrhea - Fatty stools.
- Stein-Leventhal syndrome - See Polycystic ovaries.
- Stenosis - Narrowing or stricture of any hollow structure, such as a blood vessel or bile duct.
- Stones - Hard, unyielding substances. Stones may be made in the liver, gallbladder, blood vessels or.
- Storage-pool disease - Metabolic disorder in which some substance accumulates in unusually large.
- Streptococcus pneumoniae - Pneumonia from streptoccoccal infection.
- Streptokinase treatment - Treatment with streptokinase to dissolve blood clots in hollow blood.
- Stress incontinence - Involuntary loss of urine in women that accompanies any action that suddenly.
- Stricture - Abnormal narrowing of a passage in the body. See Stenosis.
- Strip-chart recorder - Device that prints changes in electrical activity for measurement, such as EKG.
- Stroke (Cerebrovascular accident; CVA) - Sudden decrease in the blood supply to part of the.
- Subacute bacterial endocarditis (SBE) - Chronic bacterial infection of the heart valves often caused.
- Subacute hereditary tyrosinemia - Metabolic disorder characterized by an excess of tyrosine in the.
- Subacute thyroiditis - Inflammation of the thyroid gland usually following mumps, influenza or other.
- Subluxations - Incomplete or partial dislocation.
- Sympathomimetics - Drugs that mimic the effects of the sympathetic nervous system, such as adrenalin.
- Syndrome of inappropriate anti-diuretic hormone - See Diabetes insipidus.
- Syndrome - Set of symptoms that occur together.
- Synovitis - Inflammation or infection of the synovium. See Synovium.
- Synovium - Thick fluid secreted by a thin membrane surrounding a joint.
- Syphilis, late - Final, destructive stage of the disease. Symptoms can occur anywhere from 1 to 35.
- Syphilis, primary - First stage of sexually transmitted infectious syphilis. Develops approximately 3.
- Syphilis, secondary - Develops 1 to 8 weeks after the initial chancre appears. It is characterized by a.
- Syphilis - Contagious, sexually transmitted disease that causes widespread tissue destruction if not.
- Syringomelia - Condition characterized by abnormal cavities filled with liquid in the spinal cord.
- Systemic lupus erythematosus - See Lupus erythematosus, systemic.
- TRH (Thyrotropin-releasing factor) - Chemical substance secreted by the hypothalamus. Regulates.
- TSH (Thyroid-stimulating hormone) - Chemical substance secreted by the pituitary gland; controls.
- Tachycardia - Heartbeat that is too fast.
- Tay-Sachs disease - Inherited, rare disorder of the central nervous system in infants and young.
- Temporal lobe epilepsy - See Epilepsy, temporal lobe.
- Teratoma - Tumor made up of several types of different tissue, none of which is native to the area in.
- Thalassemia (Mediterranean anemia; hereditary leptocytosis) - Inherited form of anemia in.
- Thrombocytopenia - Reduction of platelets in the blood, which reduces blood clotting and increases.
- Thrombocytosis - Abnormal increase in the number of platelets. Often causes no symptoms. Usually.
- Thrombophlebitis (superficial) - Inflammation and small blood clots in a vein near the body surface.
- Thrombosis, venous (Deep-vein thrombosis) - Blood clot that forms in a vein, usually in the lower.
- Thrombosis - Blood clot in a blood vessel.
- Thrush - Infection by yeast cells of the mouth, usually in infants.
- Thymectomy - Surgical removal of the thymus gland.
- Thyroid profile - Cost is about $30.00. Blood tests performed include T3 uptake and T4 uptake. See.
- Thyroiditis - Inflammation of the thyroid gland. Acute thyroiditis is caused by a bacterial infection and.
- Thyroxine-binding globulin abnormalities - Condition in which abnormal globulins circulating in the.
- Tibio-fibular disease - Disorders of the two big bones of the leg between the knee and ankle.
- Titer - Quantity of a substance required to produce a reaction with a given volume of another.
- Tonsillitis - Inflammation of the tonsils. Tonsils are small at birth, enlarge during childhood and become.
- Tonsils - Clumps of lymphoid tissue at the back of the throat.
- Toxemia - Presence of toxins in the bloodstream. Also called blood poisoning. See Eclampsia;.
- Toxic adenoma - Small, benign nodule in the thyroid gland that secretes thyroid hormone. Cause is.
- Toxic nodular goiter - Tumor of the thyroid gland with nodules. Causes overactivity of the thyroid.
- Toxic-shock syndrome - Disease characterized by sudden onset of fever, diarrhea, vomiting, sore.
- Toxicosis - Any disease condition due to poisoning.
- Toxins - Poisons, usually produced by or occurring in a microorganism.
- Transferase deficiency - Deficiency of any group of enzymes called transferase. Transferase enzymes.
- Transferrin - Substance present in the blood. It is essential for transportation of iron from the intestine.
- Transient ischemic attacks (TIA) - Temporary decrease in blood supply to part of the brain. The.
- Translocation - Removal to another place. In genetics, the shifting of a segment or fragment of one.
- Tri-Iodothyronine (T3 3) toxicosis (Thyroid storm) - Crisis in uncontrolled hyperthyroidism.
- Tricuspid regurgitation - Abnormal flow of blood backward through the tricuspid valves.
- Tricuspid stenosis - Closure of the tricuspid valves.
- Tricuspid valves - Valves between the left ventricle and the aorta.
- Triploidy - Presence in humans of 69 chromosomes (3 full sets). Frequently causes miscarriages.
- Trisomy - Addition of a third chromosome to an otherwise normal cell.
- Trochar - Instrument with a blunt component inside a sharp tube. Used to pierce the wall of a body.
- Tropical sprue - Chronic form of malabsorption accompanied by diarrhea; occurs in the tropics and.
- Tuberculosis - Contagious, bacterial infection caused by the germ mycobacterium tuberculosis. Usually.
- Tubular epithelial damage - Damage to the lining cells of kidney tubules.
- Tubular function - Normal function of kidney tubules.
- Tularemia - Infectious bacterial disease of rodents that is transmissible to man by infected insects or.
- Tumor - New growth of tissue in which multiplication of cells is uncontrolled and progressive.
- Turner's syndrome - Chromosome abnormality seen in about 1 in 3,000 live female births. It is.
- Typhus - Disease caused by various species of rickettsia. Symptoms include fever, chills, headache.
- Ulcer - Round, crater-like lesion of the skin or mucous membrane resulting from tissue death.
- Ulcerative colitis - Serious, chronic inflammatory disease of the large intestine (colon). Characterized.
- Unconjugated bilirubin - Fat-soluble form of bilirubin that circulates in loose association with plasma.
- Uremia - Presence in blood of excessive amounts of protein metabolism byproducts, such as urea.
- Ureter - Tube that carries urine from the kidney to the bladder.
- Ureteroceles - Prolapse of the end of the ureter where it joins the bladder. Prolapse is a falling or.
- Urethra - Hollow anatomical structure that leads from the bladder to outside the body.
- Urethritis - Inflammation or infection of the urethra.
- Urogenital - Referring to the kidney and reproductive systems of the human body. Also called.
- Urokinase treatment - Treatment with the enzyme urokinase found in urine. Enzyme activates the.
- Valvular heart disease - Complication of diseases that distort or destroy heart valves. The heart has.
- Varices - Enlarged veins, arteries or lymph vessels.
- Vasculitis - Inflammation of a blood vessel.
- Vasoconstriction - State in which blood vessels are tightened or narrowed. Can be caused by the.
- Vasopressin-resistant diabetes insipidus - Diabetes insipidus that does not respond to treatment.
- Vasopressin - Hormone made by the hypothalamus and stored in the pituitary gland.
- Venous hypertension - Pressure in veins that is higher than normal.
- Venous thrombosis - Blood clot in a vein.
- Vertebral-artery disease - Disease (usually hardening of the artery) in the vertebral artery, a large.
- Vesicoureteral reflux - Condition in which urine flows backward from the bladder into the ureters.
- Vestibular - Pertaining to an oral cavity in the middle of the inner ear.
- Virilization - Process in which secondary male sexual characteristics are acquired by a female, usually.
- Visual field - Field of vision measured by special tests.
- Vitreous (Vitreous humor) - Clear fluid that fills much of the eye.
- Von Willebrand's disease - Inherited disorder characterized by abnormally slow clotting of the blood.
- Waldenstrom's macroglobulinemia - Rare, progressive disorder associated with abnormal proteins.
- Wedging - Crowding, forcing or pushing into a limited space.
- Wegener's granulomatosis - Progressive disease characterized by lesions in the bronchi and lungs.
- Whipple's disease - Malabsorption disease characterized by diarrhea, fat in the stool, skin.
- Whooping cough - Serious, contagious, bacterial infection of the bronchial tubes and lungs, most.
- Wilm's tumor - Rapidly developing malignant tumor of the kidneys in children under 5 years of age.
- Wilson's syndrome - Degeneration of the liver and the nucleus of the lens in the eye.
- Wiskott-Aldrich syndrome - Inherited immunodeficiency disorder only affecting males. Characterized.
- Wolff-Parkinson-White syndrome - Intermittent rapid heartbeat or atrial fibrillation with characteristic.
- Xanthines - Class of drugs that stimulate the brain and smooth muscles, such as bronchial tubes and the.
- Xerophthalmia - Abnormal dryness and thickening of the mucous membrane lining of the eyelids and.
- Yellow vision - Objects appear yellow. One symptom of digitalis toxicity.
- Zenker's diverticulum - Outpouching in the region where the pharynx and esophagus touch.
- Zollinger-Ellison syndrome - Syndrome with three features: severe ulcers of the stomach or small intestine.
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- 12-Hydroxyeicosatetraenoic acid
- 15q overgrowth syndrome
- 2q37 monosomy
- 3-Hydroxyisobutyryl-CoA deacylase deficiency
- 5-Hydroxyeicosatetraenoic acid
- 5-Oxo-eicosatetraenoic acid
- 580 dysentery epidemic in Gaul
- ACAM2000
- ACDC (medicine)
- AFF2
- AIDS dysmorphic syndrome
- ALS
- ATR-X syndrome
- Aarskog–Scott syndrome
- Aase syndrome
- Abdallat–Davis–Farrage syndrome
- Abdominal aura
- Abdominal compartment syndrome
- Abetalipoproteinemia
- Abnormal basal metabolic rate
- Abruzzo–Erickson syndrome
- Achard–Thiers syndrome
- Acheiropodia
- Achondroplasia
- Achondroplasia in children
- Acorn cyst sign
- Acquired generalized lipodystrophy
- Acrofrontofacionasal dysostosis
- Acromegaly
- Acromesomelic dysplasia
- Actinic conjunctivitis
- Activation syndrome
- Acute (medicine)
- Acute HME syndrome
- Acute bronchitis
- Acute chest syndrome
- Acute hemorrhagic conjunctivitis
- Acute pancreatitis
- Acute radiation syndrome
- Acute retroviral syndrome
- Acyl-CoA oxidase deficiency
- Adams–Nance syndrome
- Adams–Oliver syndrome
- Adams–Stokes syndrome
- Addison's disease
- Adducted thumb syndrome
- Adenitis
- Adenoiditis
- Adenosine deaminase 2 deficiency
- Adiposogenital dystrophy
- Adolescent idiopathic scoliosis
- Adult-onset Still's disease
- Advanced sleep phase disorder
- Aerotoxic syndrome
- Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome
- Age of onset
- Agenesis of the vena cava
- Aging-associated diseases
- Al Gazali Sabrinathan Nair syndrome
- Alabama rot
- Alagille syndrome
- Albright's hereditary osteodystrophy
- Alcohol and cancer
- Alcohol intolerance
- Alcoholic hepatitis
- Alexander disease
- Alfalfa pests
- Alien hand syndrome
- Allan–Herndon–Dudley syndrome
- Allergic response
- Allopurinol hypersensitivity syndrome
- Alopecia contractures dwarfism intellectual disability syndrome
- Alport syndrome
- Alström syndrome
- Alternating hemiplegia
- Alternating hemiplegia of childhood
- Aluminium phosphide poisoning
- Alvarez' syndrome
- Alzheimer's disease
- Amaurosis congenita, cone-rod type, with congenital hypertrichosis
- Ametropic amblyopia
- Amnion nodosum
- Amyand's hernia
- Anaplastic astrocytoma
- Anaplastic oligodendroglioma
- Animal attack
- Aniridia renal agenesis psychomotor retardation
- Anisochromia
- Anisomastia
- Anomalous left coronary artery from the pulmonary artery
- Anorectal anomalies
- Anterior compartment syndrome
- Anterior interosseous syndrome
- Anterior segment mesenchymal dysgenesis
- Antibiotic sensitivity testing
- Anticonvulsant hypersensitivity syndrome
- Antidepressant discontinuation syndrome
- Anton syndrome
- Aortic Arch Syndrome
- Aortocaval compression syndrome
- Aplasia
- Appendicitis
- Aprosencephaly cerebellar dysgenesis
- Arakawa's syndrome II
- Arginine:glycine amidinotransferase deficiency
- Aromatic L-amino acid decarboxylase deficiency
- Arteritis
- Arthritis
- Arthrogryposis multiplex with deafness, inguinal hernias, and early death
- Arthrogryposis–renal dysfunction–cholestasis syndrome
- Artificial turf–cancer hypothesis
- Ascending cholangitis
- Ascher's syndrome
- Asherman's syndrome
- Ashman phenomenon
- Asthma
- Asthma-COPD overlap
- Asymptomatic carrier
- Atelosteogenesis type I
- Atherosclerosis
- Athletic heart syndrome
- Atony
- Atresia
- Atrophic gastritis
- Atrophic vaginitis
- Atypical hemolytic uremic syndrome
- Atypical pulmonary carcinoid tumour
- Auditory processing disorder
- Autoimmune polyendocrine syndrome type 1
- Autoimmune polyendocrine syndrome type 2
- Autoimmune polyendocrine syndrome type 3
- Autophagic vacuolar myopathy
- Autosomal dominant cerebellar ataxia, deafness, and narcolepsy
- Autosomal dominant partial epilepsy with auditory features
- Autosomal dominant porencephaly type I
- Autosomal recessive axonal neuropathy with neuromyotonia
- Autosomal recessive bestrophinopathy
- Avellis syndrome
- Avulsion injury
- Axillary lymphadenopathy
- Azzopardi phenomenon
- Bacillary peliosis
- Bainbridge–Ropers syndrome
- Balanitis
- Balanitis circinata
- Baller–Gerold syndrome
- Bangstad syndrome
- Barbiturate dependence
- Bare lymphocyte syndrome
- Barrier nursing
- Barré–Liéou syndrome
- Bart syndrome
- Barton's fracture
- Bart–Pumphrey syndrome
- Basopenia
- Batten disease
- Battle's sign
- Baylisascaris
- Behçet's disease
- Benign acute childhood myositis
- Benign hereditary chorea
- Berk–Tabatznik syndrome
- Berlin's edema
- Bethlem myopathy
- Bhaskar–Jagannathan syndrome
- Bifid nose
- Bilateral frontoparietal polymicrogyria
- Biliary fever
- Biliary fistula
- Biliary injury
- Biliary pseudolithiasis
- Bill of health
- Bimalleolar fracture
- Binder's syndrome
- Biotin-thiamine-responsive basal ganglia disease
- Biphasic disease
- Biphenotypic sinonasal sarcoma
- Black rot
- Blackheart (plant disease)
- Bladder stone (animal)
- Blain (animal disease)
- Blast injury
- Bleb (medicine)
- Blennorrhea
- Blepharitis
- Blepharophimosis-ptosis-esotropia-syndactyly-short stature syndrome
- Blight
- Blind loop syndrome
- Blood-borne disease
- Bloom syndrome
- Blue waffle
- Blue-cone monochromacy
- Blunt trauma
- Body fat redistribution syndrome
- Body load
- Bogart–Bacall syndrome
- Bone health
- Borderline tumor
- Boron deficiency (medicine)
- Bosch-Boonstra-Schaaf optic atrophy syndrome
- Bosworth fracture
- Botryoid odontogenic cyst
- Brachial amelia, cleft lip, and holoprosencephaly
- Brain abscess
- Branched-chain keto acid dehydrogenase kinase deficiency
- Breast cyst
- Brody myopathy
- Bronchiolitis
- Brooke Greenberg
- Bruise
- Bumper fracture
- Burning feet syndrome
- Burning mouth syndrome
- Burnside–Butler syndrome
- Bursitis
- Busch fracture
- Buschke–Ollendorff syndrome
- CACNA1C-related disorders
- CADASIL
- CAPP-Seq
- CD4+ T cells and antitumor immunity
- CDKL5 deficiency disorder
- CHAI disease
- CHDI Foundation
- COAT platelet defect
- COVID-19 and cancer
- CREST syndrome
- Calcific tendinitis
- Calcinosis
- Calculus (medicine)
- Camptocormia
- Camptodactyly-arthropathy-coxa vara-pericarditis syndrome
- Cancer
- Cancer Likelihood in Plasma
- Cancer and nausea
- Cancer associated retinopathy
- Cancer in Ghana
- Cancer insurance
- Cancer prevention
- Cancer research
- Cancer selection
- Cancer signs and symptoms
- Cancer survival rates
- Cancer systems biology
- Cancer treatment
- Cancer-associated fibroblast
- Cancer/testis antigens
- Canities subita
- Canker
- Cannabinoid hyperemesis syndrome
- Carbamate poisoning
- Cardiocranial syndrome, Pfeiffer type
- Cardiovascular disease
- Cardiovascular disease in Nepal
- Cardiovascular syndrome
- Cat bite
- Cataract
- Cataract-microcornea syndrome
- Catarrh
- Catastrophic antiphospholipid syndrome
- Catastrophic illness
- Catastrophic injury
- Catheter-associated urinary tract infection
- Cause (medicine)
- Cause of obsessive–compulsive disorder
- Causes and origins of Tourette syndrome
- Causes of Parkinson's disease
- Causes of cancer
- Causes of cancer pain
- Causes of mental disorders
- Causes of seizures
- Cell-mediated immunity
- Cellular Inhibitor of Apoptosis Protein 1
- Cellulitis
- CendR
- Central centrifugal cicatricial alopecia
- Central nervous system syndrome
- Central nervous system tumor
- Centrilobular necrosis
- Cerebellar abiotrophy
- Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
- Cerebral creatine deficiency
- Cerebral vasculitis
- Cerebroretinal microangiopathy with calcifications and cysts
- Cervicitis
- Cervicocranial syndrome
- Chalkstick fracture
- Chattering teeth
- Chemical colitis
- Chemosis
- Chemotherapy-induced peripheral neuropathy
- Chest photofluorography
- Chiari malformation
- Chiari–Frommel syndrome
- Child psychopathology
- Child sexual abuse accommodation syndrome
- Childhood granulomatous periorificial dermatitis
- Childhood tumor syndrome
- Chills
- Chlorellosis
- Cholecystitis
- Chondrodysplasia, Grebe type
- Chorioamnionitis
- Choroideremia
- Chromatin remodeling
- Chronic actinic dermatitis
- Chronic atrophic rhinitis
- Chronic condition
- Chronic deciduitis
- Chronic enteropathy associated with SLCO2A1 gene
- Chronic multifocal Langerhans cell histiocytosis
- Chronic obstructive pulmonary disease
- Chronic wasting disease
- Chyloderma
- Ciliopathy
- Circulating tumor DNA
- Claire Wineland
- Climate change and infectious diseases
- Climber's finger
- Climbing injuries
- Clinical endocannabinoid deficiency syndrome
- Clinophilia
- Cobb syndrome
- Coccidia
- Cockayne syndrome
- Codon reassignment
- Coeliac disease
- Coinfection
- Cold chill
- Cold compression therapy
- Cold sensitivity
- Colitis
- Collagen loss
- Collagen-induced arthritis
- Collective cell migration
- Colonic ulcer
- Combined immunodeficiencies
- Common cold
- Common variable immunodeficiency
- Community-acquired pneumonia
- Comorbidity
- Compartment syndrome
- Complement 2 deficiency
- Complement deficiency
- Complete androgen insensitivity syndrome
- Complications of prolonged standing
- Component causes
- Computer vision syndrome
- Computer-induced medical problems
- Concrescence
- Concussions in American football
- Concussions in sport
- Condensing osteitis
- Condylar resorption
- Congenital adrenal hyperplasia due to 17α-hydroxylase deficiency
- Congenital amegakaryocytic thrombocytopenia
- Congenital cartilaginous rest of the neck
- Congenital fiber type disproportion
- Congenital hemolytic anemia
- Congenital hypoplastic anemia
- Congenital insensitivity to pain
- Congenital limb deformities
- Conjunctivitis
- Constrictive pericarditis
- Contagious disease
- Copper deficiency
- Cord colitis syndrome
- Cordon sanitaire (medicine)
- Cornea plana 1
- Cornea plana 2
- Cornelia de Lange syndrome
- Coronary artery disease
- Coronary steal
- Cotton fever
- Cowpox
- Cramp fasciculation syndrome
- Cranberry fruit rot
- Cranio-lenticulo-sutural dysplasia
- Craniocervical instability
- Craniometaphyseal dysplasia
- Craniorhiny
- Cranioschisis
- Craniosynostosis and dental anomalies
- Craniosynostosis with anomalies of the cranial base and digits
- Craniosynostosis, Adelaide type
- Craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome
- Craniosynostosis-fibular aplasia syndrome
- Craniosynostosis–anal anomalies–porokeratosis syndrome
- Creatine transporter defect
- Critical community size
- Crohn's disease
- Crouzonodermoskeletal syndrome
- Crush injury
- Crush syndrome
- Cruveilhier-Baumgarten syndrome
- Cruveilhier–Baumgarten disease
- Cryoimmunotherapy
- Cryptitis
- Cryptophthalmos
- Cryptotia
- Crystallopathy
- Cuboid syndrome
- Cuffitis
- Cuneiform fracture
- Custom-made medical device
- Cyst
- Cystitis cystica
- Cytochrome P450 oxidoreductase deficiency
- Cytomegalic inclusion body disease
- Cytomegalovirus esophagitis
- Cytopenia
- Cytoreductive surgery
- DCAP-BTLS
- DNA repair-deficiency disorder
- DOCK8 deficiency
- Dacryoadenitis
- Dactylitis
- Daentl Townsend Siegel syndrome
- Damping off
- Darier's disease
- De Quervain syndrome
- Dead arm syndrome
- Death by vending machine
- Defense wound
- Deficiency (medicine)
- Degenerative disease
- Degenerative suspensory ligament desmitis
- Degloving
- Dehydration
- Delayed milestone
- Delayed sleep phase disorder
- Dementia
- Dementia with Lewy bodies
- Dent's disease
- Dental abscess
- Dermatomyositis
- Dermatoosteolysis, Kirghizian type
- Dermatopolymyositis
- Descending perineum syndrome
- Desmin-related myofibrillar myopathy
- Dietary inflammatory index
- Diffuse idiopathic skeletal hyperostosis
- Diffuse infiltrative lymphocytosis syndrome
- Diffuse leptomeningeal glioneuronal tumor
- Diogenes syndrome
- Diplomatic illness
- Dipygus
- Discitis
- Discovery of disease-causing pathogens
- Disease
- Disease cluster
- Disease mongering
- Disease outbreak
- Disease package
- Disease resistance
- Disease vector
- Diseases and epidemics of the 19th century
- Diseases of abnormal polymerization
- Diseases of affluence
- Diseases of poverty
- Disfigurement
- Dislocation of hip in animals
- Disseminated disease
- Distal hereditary motor neuropathy type V
- Distal spinal muscular atrophy type 2
- Distal trisomy 10q
- Distichiasis, congenital heart defects and mixed peripheral vascular anomalies
- Dopamine dysregulation syndrome
- Down syndrome
- Drug-induced autoimmune hemolytic anemia
- Drug-induced nonautoimmune hemolytic anemia
- Dryness (medical)
- Duane-radial ray syndrome
- Dunnigan familial partial lipodystrophy
- Duodenal lymphocytosis
- Dutch hypothesis
- Dwarfism
- Dwarfism, low-birth-weight type with unresponsiveness to growth hormone
- Dysacusis
- Dysbiosis
- Dysgammaglobulinemia
- Dyslalia
- Dysorthography
- Dysosteosclerosis
- Dyssynergia
- EPPO Code
- EUROCAT (medicine)
- EWS/FLI
- Eagle syndrome
- Echinococcus multilocularis
- Ectopic testis
- Ectopic ureter
- Ectrodactyly with tibia aplasia/hypoplasia
- Effects of long-term benzodiazepine use
- Effort incontinence
- Einstein syndrome
- Ejaculation disorders
- Electrical injury
- Electrocution
- Elliptocyte
- Eluru outbreak
- Emberger syndrome
- Emerging infectious disease
- Emphysematous cystitis
- Encapsulating peritoneal sclerosis
- Encephalitis
- Endaural phenomena
- Endocapillary proliferative glomerulonephritis
- Endocarditis
- Endogenous infection
- Endometritis
- Endotheliitis
- Enteritis
- Enterocolitis
- Enteropathic arthropathy
- Enteropathy
- Enterotoxin type B
- Entomophobia
- Environmental dependency syndrome
- Environmental disease
- Environmental factor
- Eosinophilia–myalgia syndrome
- Eosinophilic cystitis
- Eosinophilic fasciitis
- Epiblepharon
- Epicondylitis
- Epidemiology of syphilis
- Epididymal cyst
- Epididymitis
- Epigenetic clock
- Epilepsy in animals
- Epilepsy syndromes
- Epileptic spasms
- Epiploic appendagitis
- Episcleritis
- Episodic dyscontrol syndrome
- Epizootic
- Epoxydocosapentaenoic acid
- Epoxyeicosatetraenoic acid
- Epoxyeicosatrienoic acid
- Epoxygenase
- Erdheim–Chester disease
- Erondu–Cymet syndrome
- Erucin
- Esophageal motility disorder
- Esophagitis
- Esthiomene
- Evolution of Infectious Disease
- Excess ovarian androgen release syndrome
- Exothrix
- Experimental Bacteriology
- Exposure keratopathy
- Extra-Terrestrial Exposure Law
- Extramammary Paget's disease
- Extrapyramidal symptoms
- Extraskeletal myxoid chondrosarcoma
- Eye disease
- FATCO
- FET protein family
- Fabry disease
- Factitious disorder imposed on another
- Failure to thrive
- Falling (accident)
- Falls in older adults
- Familial cirrhosis
- Familial dwarfism and painful muscle spasms
- Familial dysautonomia
- Familial multiple intestinal atresia
- Familial opposable triphalangeal thumbs duplication
- Familial osteodysplasia, Anderson type
- Familial partial lipodystrophy
- Familial renal amyloidosis
- Fanconi syndrome
- Farber disease
- Fares Scale of Injuries due to Cluster Munitions
- Fasciitis
- Fasciola gigantica
- Fasciola hepatica
- Fasciolosis
- Fauces (throat)
- Fazio–Londe disease
- Febrile neutrophilic dermatosis
- Femur fibula ulna syndrome
- Fertility preservation
- Fetal alcohol spectrum disorder
- Fetal hydantoin syndrome
- Fetal warfarin syndrome
- Fever
- Fever of unknown origin
- Fibrinogenolysis
- Fibrinolysis syndrome
- Fibroblastic and myofibroblastic tumors
- Fibromyalgia syndrome
- Fibrosing colonopathy
- Fibrosis
- Filariasis
- Filippi syndrome
- First arch syndrome
- Fistula
- Flammer syndrome
- Floppy eyelid syndrome
- Florid cutaneous papillomatosis
- Flying glass
- Focal proliferative nephritis
- Foix–Chavany–Marie syndrome
- Follicle-stimulating hormone insensitivity
- Fomite
- Forbes-Albright syndrome
- Foreign animal disease
- Forma specialis
- Fragile X-associated primary ovarian insufficiency
- Fraser syndrome
- Frasier syndrome
- Fratricidins
- Fresh water skin disease
- Freshers' flu
- Friability
- Froin's syndrome
- Frontal horn cyst
- Fuchs' dystrophy
- Fumigatory box
- Functional disorder
- Fungal pneumonia
- Fusarium
- Fusarium oxysporum
- GATAD2B-associated neurodevelopmental disorder
- GOSR2-related progressive myoclonus ataxia
- Gartner's duct cyst
- Gastritis
- Gastrocutaneous syndrome
- Gastroenteritis
- Gastrointestinal syndrome
- Gaucher's disease
- Generalized arterial calcification of infancy
- Genetic disorder
- Genetics of GnRH deficiency conditions
- Genital trauma
- Genitourinary amoebiasis
- Genitourinary tract injury
- Genome instability
- Germ theory of disease
- Giant-cell fibroma
- Giardiasis
- Gigantism
- Gingivitis
- Gleich's syndrome
- Glenolabral articular disruption
- Glioblastoma
- Global Genes
- Global Viral
- Globalization and disease
- Glomerular hyperfiltration
- Glomerulonephritis
- Glomerulopathy
- Glossitis
- Glucocorticoid resistance
- Glutaminase deficiency
- Glycogen storage disease type IX
- Glycogenic hepatopathy
- Gnathitis
- Golfer's vasculitis
- Gollop-Wolfgang complex
- Gonadotropin insensitivity
- Gonadotropin-releasing hormone insensitivity
- Gougerot–Blum syndrome
- Gouverneur's syndrome
- Gradenigo's syndrome
- Graham-Little syndrome
- Graham–Boyle–Troxell syndrome
- Granular myringitis
- Granuloma
- Gray baby syndrome
- Greater trochanteric pain syndrome
- Green Tobacco Sickness
- Green nail syndrome
- Grinspan's syndrome
- Griscelli syndrome type 2
- Griscelli syndrome type 3
- Grisel's syndrome
- Growing teratoma syndrome
- Growth hormone deficiency
- Guard theory
- Guillain–Barré syndrome
- Gulf War syndrome
- Gunshot wound
- HEC syndrome
- HFE H63D gene mutation
- HHH syndrome
- HIV/AIDS
- HPV-associated oropharyngeal cancer awareness and prevention
- Haab's striae
- Haglund's syndrome
- Hailey–Hailey disease
- Hair tourniquet
- Halal syndrome
- Hamman's syndrome
- Hamman-Rich syndrome
- Hangnail
- Haploinsufficiency of A20
- Harris platelet syndrome
- Hashimoto's thyroiditis
- Haverhill fever
- Head pressing
- Headache
- Healing
- Health problems of musicians
- Heart failure
- Heat intolerance
- Heavy legs
- Heel pad syndrome
- Heel spur syndrome
- Hemihyperplasia–multiple lipomatosis syndrome
- Hemihypertrophy
- Hemispatial neglect
- Hemoglobin Lepore syndrome
- Hemoglobin O
- Hennekam syndrome
- Hepatitis
- Hepatitis X
- Hepatoid tumor
- Hepatolithiasis
- Hereditary diffuse leukoencephalopathy with spheroids
- Hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis
- Hereditary gingival fibromatosis
- Hereditary haemochromatosis
- Hereditary hyperbilirubinemia
- Hereditary neuralgic amyotrophy
- Herpetic gingivostomatitis
- Heterogeneous condition
- Hexokinase deficiency
- Hickey
- Hidradenitis suppurativa
- High pressure injection injury
- High-arched palate
- Histidinuria renal tubular defect syndrome
- History of chronic fatigue syndrome
- Hodgkin lymphoma
- Holdsworth fracture
- Holiday heart syndrome
- Holoendemic
- Homogeneously staining region
- Honeymoon rhinitis
- Hopkins syndrome
- Horizontal gaze palsy
- Horizontal transmission
- Hospital-acquired infection
- Hospital-acquired pneumonia
- Host factor
- Howel–Evans syndrome
- Ho–Kaufman–Mcalister syndrome
- Hughes–Stovin syndrome
- Human Growth Foundation
- Human Pathogens and Toxins Act
- Human somatic variation
- Human-to-human transmission
- Human-to-primate transmission
- Hunter syndrome
- Huntington's disease
- Hurler syndrome
- Hurler–Scheie syndrome
- Hutchinson's triad
- Hydremia
- Hyperchlorhydria
- Hyperendemic
- Hyperglycerolemia
- Hypermobility (joints)
- Hyperosmolar syndrome
- Hyperprolactinaemia
- Hyperprolactinemic SAHA syndrome
- Hyperproteinemia
- Hyperprothrombinemia
- Hyperspermia
- Hypertension and brachydactyly syndrome
- Hypertension and the brain
- Hypertrichosis cubiti
- Hyperventilation syndrome
- Hyperviscosity syndrome
- Hypnozygote
- Hypochondroplasia
- Hypodysfibrinogenemia
- Hypohidrotic ectodermal dysplasia
- Hypophysitis
- Hypoplasminogenemia
- Hypoplastic right heart syndrome
- Hypotonia
- Hypotrichosis–acro-osteolysis–onychogryphosis–palmoplantar keratoderma–periodontitis syndrome
- Hypotrichosis–lymphedema–telangiectasia syndrome
- Hystrix-like ichthyosis–deafness syndrome
- ICD coding for rare diseases
- Ichthyosis follicularis with alopecia and photophobia syndrome
- Ichthyosis-intellectual disability-dwarfism-renal impairment
- Idiopathic chronic fatigue
- Idiopathic disease
- Idiopathic giant-cell myocarditis
- Idiopathic granulomatous hepatitis
- Idiopathic hypercalcinuria
- Idiopathic interstitial pneumonia
- Idiopathic multicentric Castleman disease
- Idiopathic pulmonary fibrosis
- Idiopathic pure sudomotor failure
- Idiopathic short stature
- Ileitis
- Ileosigmoid knot
- Iliocostal friction syndrome
- Iliotibial band syndrome
- Immune reconstitution inflammatory syndrome
- Immune thrombocytopenic purpura
- Immune-mediated inflammatory diseases
- Immunization during pregnancy
- Immunodeficiency 26
- Impaction (animals)
- Imposex
- Inborn errors of steroid metabolism
- Inclusion body myositis
- Incubation period
- Indian Genetic Disease Database
- Ineffective erythropoiesis
- Infant and toddler safety
- Infant respiratory distress syndrome
- Infantile cerebellar retinal degeneration
- Infantile cortical hyperostosis
- Infantile digital fibromatosis
- Infantile speech
- Infection
- Infection prevention and control
- Infection rate
- Infections associated with diseases
- Infectious Disease (Notification) Act 1889
- Infectious causes of cancer
- Infectious diseases (athletes)
- Infectious diseases (medical specialty)
- Infectious period
- Infertility in polycystic ovary syndrome
- Infiltrative ophthalmopathy
- Inflammaging
- Inflammation
- Inflammatory demyelinating diseases of the central nervous system
- Inflammatory fibroid polyp
- Influenza-like illness
- Inguinal lymphadenopathy
- Inherited thrombotic thrombocytopenic purpura
- Injury
- Injury in humans
- Insulitis
- Intellectual disability-spasticity-ectrodactyly syndrome
- Internal bleeding
- International Cocoa Quarantine Centre
- International Sanitary Conferences
- Intertrigo
- Interventional oncology
- Intestinal infectious diseases
- Intraarticular fracture
- Intracapsular fracture
- Intracellular bacteria
- Intracranial epidermoid cyst
- Intracranial hypertension syndrome
- Intraductal papillary neoplasm of the bile duct
- Intraretinal microvascular abnormalities
- Intravenous marijuana syndrome
- Invasive urothelial carcinoma
- Iridocorneal endothelial syndrome
- Iris hypoplasia with glaucoma
- Irlen syndrome
- Irregular sleep–wake rhythm disorder
- Irritation
- Irritation fibroma
- Irukandji syndrome
- Irvine–Gass syndrome
- Isolated growth hormone deficiency
- Isolated hyperCKemia
- Isolation (health care)
- Isolation ward
- Jansen's metaphyseal chondrodysplasia
- Jansky–Bielschowsky disease
- Jeavons syndrome
- Johnson–Munson syndrome
- Juvenile idiopathic arthritis
- Juvenile myoclonic epilepsy
- Juvenile nephronophthisis
- KCNQ2 developmental and epileptic encephalopathy
- Kawasaki disease
- Kennel cough
- Keratic precipitate
- Keratitis
- Keratoconjunctivitis
- Keratosis linearis with ichthyosis congenita and sclerosing keratoderma syndrome
- Keratosis pilaris
- Ketosis-prone diabetes
- Kibong'oto Hospital
- Killian–Jamieson diverticulum
- Kimmelstiel-Wilson syndrome
- Klinefelter syndrome
- Knee arthritis
- Knobloch syndrome
- Koch's postulates
- Kowarski syndrome
- Krabbe disease
- Kufor–Rakeb syndrome
- König's syndrome
- LPS-responsive beige-like anchor protein deficiency
- LRBA deficiency
- Laboratory-acquired infection
- Labyrinthitis
- Lace bite
- Lafora disease
- Laminopathy
- Landau–Kleffner syndrome
- Langer–Giedion syndrome
- Laron syndrome
- Laryngitis
- Late effect
- Late life depression
- Late onset congenital adrenal hyperplasia
- Latent period (epidemiology)
- Lazarus syndrome
- Leaky gut syndrome
- Legius syndrome
- Leigh syndrome
- Leiner's disease
- Lenz–Majewski syndrome
- Leprosy
- Leriche's syndrome
- Leschke syndrome
- Lethal congenital contracture syndrome
- Lethal dwarfism in rabbits
- Letterer–Siwe disease
- Leucosis
- Leukotriene receptor antagonist-associated Churg–Strauss syndrome
- Levator ani syndrome
- Levocardia
- Leydig cell hypoplasia
- Lifestyle disease
- Ligneous conjunctivitis
- Lima syndrome
- Limb girdle syndrome
- Limbal nodule
- Linburg–Comstock variation
- Lions Eye Institute
- Lipoatrophy
- Lisch epithelial corneal dystrophy
- List of Legionnaires' disease outbreaks
- List of OMIM disorder codes
- List of Rift Valley fever outbreaks
- List of WHO fungal priority pathogens
- List of anthrax outbreaks
- List of autoimmune diseases
- List of awareness ribbons
- List of biological development disorders
- List of cancer types
- List of causes of shortness of breath
- List of childhood diseases and disorders
- List of circulatory system conditions
- List of countries by cancer deaths
- List of countries by cancer rate
- List of cryptosporidiosis outbreaks
- List of diseases (0–9)
- List of diseases (A)
- List of diseases (B)
- List of diseases (C)
- List of diseases (D)
- List of diseases (E)
- List of diseases (F)
- List of diseases (G)
- List of diseases (H)
- List of diseases (I)
- List of diseases (J)
- List of diseases (K)
- List of diseases (L)
- List of diseases (M)
- List of diseases (N)
- List of diseases (O)
- List of diseases (P)
- List of diseases (Q)
- List of diseases (R)
- List of diseases (S)
- List of diseases (T)
- List of diseases (U)
- List of diseases (V)
- List of diseases (W)
- List of diseases (X)
- List of diseases (Y)
- List of diseases (Z)
- List of diseases by year of discovery
- List of diseases eliminated from the United States
- List of diseases spread by invertebrates
- List of disorders
- List of epidemics and pandemics
- List of eponymous diseases
- List of fetal abnormalities
- List of fibrinogen disorders
- List of fictional diseases
- List of foodborne illness outbreaks
- List of foodborne illness outbreaks by death toll
- List of genetic disorders
- List of hematologic conditions
- List of human disease case fatality rates
- List of infections of the central nervous system
- List of infectious diseases
- List of infectious diseases causing flu-like syndrome
- List of inflammatory disorders
- List of language disorders
- List of mental disorders
- List of neurological conditions and disorders
- List of notifiable diseases
- List of parasites of humans
- List of pathogens by size
- List of pollution-related diseases
- List of rare disease organisations
- List of skin conditions
- List of syndromes
- List of systemic diseases with ocular manifestations
- List of types of inflammation by location
- List of types of malnutrition
- Lists of diseases
- Little People of America
- Li–Fraumeni syndrome
- Local gigantism
- Localized disease
- Locked-in syndrome
- Loin pain hematuria syndrome
- Loose anagen syndrome
- Low anterior resection syndrome
- Low-grade fibromyxoid sarcoma
- Low-grade myofibroblastic sarcoma
- Lower respiratory tract infection
- Lucey–Driscoll syndrome
- Ludwig's angina
- Lund and Browder chart
- Lupus vasculitis
- Lymph node metastasis
- Lymphadenopathy
- Lymphatic malformation 6 syndrome
- Lymphedema–distichiasis syndrome
- Lymphocytic colitis
- Lynch Syndrome
- Lysosomal acid lipase deficiency
- Léri–Weill dyschondrosteosis
- MAGIC Foundation
- MEDNIK syndrome
- MELAS syndrome
- Macrocephaly-capillary malformation
- Macrodystrophia lipomatosa
- Macrophage activation syndrome
- Maculopathy
- Mad cow crisis
- Majeed syndrome
- Majewski's polydactyly syndrome
- Malaise
- Male genital disease
- Malformative syndrome
- Mallory–Weiss syndrome
- Malnutrition–inflammation complex
- Management of acute coronary syndrome
- Manning criteria
- Mannosidosis
- Marinesco–Sjögren syndrome
- Mast cell activation syndrome
- Mastitis
- Mastocytoma in dogs
- Mastoiditis
- Maxwell Finland Award
- Maydl's hernia
- Mayer–Rokitansky–Küster–Hauser syndrome
- May–White syndrome
- Mazzotti reaction
- McArdle syndrome
- McCune–Albright syndrome
- McCusick syndrome
- McKittrick–Wheelock syndrome
- Mean world syndrome
- MecA
- Mechanical anisocoria
- Meckel–Gruber syndrome
- Meconium aspiration syndrome
- Median palatal cyst
- Medical geography
- Medicinal fungi
- Megalocornea
- Megarectum
- Megaureter
- Megavitamin-B6 syndrome
- Melanocytic tumor
- Melanoma
- Melanotic neuroectodermal tumor of infancy
- Meltzer's triad
- Membranous glomerulonephritis
- Mendelian susceptibility to mycobacterial disease
- Menkes disease
- Mensacarcin
- Meromelia
- Mesenteric cyst
- Mesenteric pseudocyst
- Mesomelia
- Mesothelial hyperplasia
- Metallosis
- Metaphyseal chondrodysplasia Schmid type
- Methaemalbuminaemia
- Methylenetetrahydrofolate dehydrogenase 1 deficiency
- Metropathia haemorrhagica
- MiR-206
- Michelin tire baby syndrome
- Microbial pathogenesis
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