Portal:Medicine
From WikiMD's Health & Wellness Encyclopedia
Medicine is the science and practice of establishing the diagnosis, prognosis, treatment, and prevention of disease. Medicine encompasses a variety of health care practices evolved to maintain and restore health by the prevention and treatment of illness. Contemporary medicine applies biomedical sciences, biomedical research, genetics, and medical technology to diagnose, treat, and prevent injury and disease, typically through pharmaceuticals or surgery, but also through therapies as diverse as psychotherapy, external splints and traction, medical devices, biologics, and ionizing radiation, amongst others.
Medicine as field of study[edit | edit source]
Medicine is the scientific study and clinical practice of diagnosing, treating, and preventing diseases and injuries. It comprises a wide range of disciplines, including internal medicine, surgery, pediatrics, and psychiatry, among many others, and is a profession that is always evolving and diversified.
Branches of medicine[edit | edit source]
The primary branches of medicine are the basic sciences and the clinical sciences.
Basic sciences[edit | edit source]
Anatomy, physiology, pharmacology, and immunology are the basis of medical knowledge and are included in the basic sciences. This information is crucial for comprehending illness mechanisms and developing new remedies.
Clinical sciences[edit | edit source]
]]Clinical sciences]], on the other hand, are concerned with the diagnostic and therapeutic applications of fundamental scientific knowledge. This encompasses internal medicine, surgery, pediatrics, as well as obstetrics and gynecology.
Online textbook of medicine[edit | edit source]
WikiMD's free online textbook of medicine covers topics such as anatomy, physiology, neurology, pharmacology, pathology, surgery, radiology, epidemiology, and many other subjects. Each chapter would provide detailed information on the specific topic and include illustrations, diagrams, and case studies to help students understand and apply the material.
Alphabetic listing of common topics[edit | edit source]
Table of contents:
.A | .B | .C | .D | .E | .F | .G | .H | .I | .J | .K | .L | .M
.N | .O | .P | .Q | .R | .S | .T | .U | .V | .W | .X | .Y | .Z
A[edit | edit source]
- 17q12 deletion syndrome
- 17q12 duplication
- 1p36 deletion syndrome
- 21 hydroxylase deficiency
- 2q37 deletion syndrome
- 3 beta hydroxysteroid dehydrogenase deficiency
- 3 methylcrotonyl coa carboxylase deficiency
- 3p deletion syndrome
- 3q29 microdeletion syndrome
- 5 alpha reductase deficiency
- 5q minus syndrome
- Abdominal wall defect
- Abetalipoproteinemia
- Abortion
- Abscess
- Acatalasemia
- Aceruloplasminemia
- Achondrogenesis
- Achondroplasia
- Achromatopsia
- Acne
- Acral peeling skin syndrome
- Acrocallosal syndrome
- Acromicric dysplasia
- Acupuncture
- Acute promyelocytic leukemia
- Adenine phosphoribosyltransferase deficiency
- Adenoids
- Adenosine deaminase 2 deficiency
- Adenosine deaminase deficiency
- Adenosine monophosphate deaminase deficiency
- Adenylosuccinate lyase deficiency
- Adermatoglyphia
- Adhesions
- Adiposis dolorosa
- Adult polyglucosan body disease
- African iron overload
- Age related macular degeneration
- Aicardi syndrome
- Alagille syndrome
- Albanian
- Alcohol use disorder
- Alcohol
- Alexander disease
- Alkaline phosphatase
- Alkaptonuria
- Allergic asthma
- Allergy
- Alopecia areata
- Alpha 1 antitrypsin deficiency
- Alpha mannosidosis
- Alpha thalassemia
- Alport syndrome
- Alstrom syndrome
- Alternating hemiplegia of childhood
- Alzheimer disease
- Amblyopia
- Amelogenesis imperfecta
- Amharic
- Aminoacylase 1 deficiency
- Amish lethal microcephaly
- Amyloidosis
- Amyotrophic lateral sclerosis
- Anaphylaxis
- Anatomy
- Anauxetic dysplasia
- Andermann syndrome
- Androgen insensitivity syndrome
- Androgenetic alopecia
- Anemia
- Anencephaly
- Anesthesia
- Aneurysms
- Angelman syndrome
- Angina
- Angioplasty
- Aniridia
- Ankylosing spondylitis
- Anoscopy
- Anthrax
- Antibiotics
- Antidepressants
- Antioxidants
- Antiphospholipid syndrome
- Anxiety
- Apert syndrome
- Aphasia
- Appendicitis
- Arabic
- Arginase deficiency
- Argininosuccinic aciduria
- Armenian
- Aromatase deficiency
- Aromatase excess syndrome
- Arrhythmia
- Arrhythmogenic right ventricular cardiomyopathy
- Arsenic
- Arterial tortuosity syndrome
- Arthritis
- Arts syndrome
- Asbestos
- Aspartylglucosaminuria
- Aspergillosis
- Asphyxiating thoracic dystrophy
- Asthma
- Ataxia telangiectasia
- Atelosteogenesis type 1
- Atelosteogenesis type 2
- Atelosteogenesis type 3
- Atherosclerosis
- Atopic dermatitis
- Attention deficit hyperactivity disorder
- Atypical hemolytic uremic syndrome
- Autism spectrum disorder
- Autoimmune lymphoproliferative syndrome
- Autosomal dominant leukodystrophy with autonomic disease
- Autosomal dominant nocturnal frontal lobe epilepsy
- Autosomal dominant partial epilepsy with auditory features
- Autosomal recessive axonal neuropathy with neuromyotonia
- Autosomal recessive cerebellar ataxia type 1
- Autosomal recessive primary microcephaly
B[edit | edit source]
Table of contents:
.A | .B | .C | .D | .E | .F | .G | .H | .I | .J | .K | .L | .M
.N | .O | .P | .Q | .R | .S | .T | .U | .V | .W | .X | .Y | .Z
- Barium swallow
- Barotrauma
- Barth syndrome
- Bartter syndrome
- Beckwith wiedemann syndrome
- Bedbugs
- Behcet disease
- Bengali
- Benign essential blepharospasm
- Benign familial neonatal seizures
- Benign recurrent intrahepatic cholestasis
- Bereavement
- Beta ketothiolase deficiency
- Beta mannosidosis
- Beta thalassemia
- Biopsy
- Biotinidase deficiency
- Bipolar disorder
- Birt hogg dube syndrome
- Birthmarks
- Birthweight
- Bjornstad syndrome
- Bladder cancer
- Blau syndrome
- Bleeding
- Blisters
- Blood in urine
- Blood smear
- Blood
- Bloom syndrome
- Bohring opitz syndrome
- Boomerang dysplasia
- Bosnian
- Botox
- Botulism
- Breast biopsy
- Breast cancer
- Breastfeeding
- Brody myopathy
- Brugada syndrome
- Bruises
- Bunion
- Burmese
- Bursitis
C[edit | edit source]
Table of contents:
.A | .B | .C | .D | .E | .F | .G | .H | .I | .J | .K | .L | .M
.N | .O | .P | .Q | .R | .S | .T | .U | .V | .W | .X | .Y | .Z
- Caffeine
- Caffey disease
- Calcium
- Campomelic dysplasia
- Canavan disease
- Cancer
- Cancers
- Cantu syndrome
- Cap myopathy
- Carbamoyl phosphate synthetase I deficiency
- Carbohydrates
- Cardiofaciocutaneous syndrome
- Cardiomyopathy
- Caregivers
- Carney complex
- Carnitine acylcarnitine translocase deficiency
- Carnitine palmitoyltransferase I deficiency
- Carpal tunnel syndrome
- Carpenter syndrome
- Cartilage hair hypoplasia
- Cataract
- Catecholaminergic polymorphic ventricular tachycardia
- Caudal regression syndrome
- Celiac disease
- Cellulitis
- Central core disease
- Centronuclear myopathy
- Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
- Cerebral cavernous malformation
- Cerebrotendinous xanthomatosis
- Char syndrome
- Charge syndrome
- Chediak higashi syndrome
- Cherubism
- Chickenpox
- Chikungunya
- Childbirth
- Childhood absence epilepsy
- Chiropractic
- Choking
- Cholangiocarcinoma
- Cholera
- Cholesterol
- Chordoma
- Chorea acanthocytosis
- Choroideremia
- Christianson syndrome
- Chronic granulomatous disease
- Chronic myeloid leukemia
- Chuukese
- Chylomicron retention disease
- Circumcision
- Cirrhosis
- Citrullinemia
- Cleidocranial dysplasia
- Cloning
- Clouston syndrome
- Cocaine
- Cockayne syndrome
- Coffin lowry syndrome
- Coffin siris syndrome
- Cohen syndrome
- Coloboma
- Colonoscopy
- Color vision deficiency
- Colposcopy
- Coma
- Common variable immune deficiency
- Complement component 2 deficiency
- Complement component 8 deficiency
- Concussion
- Congenital afibrinogenemia
- Congenital bilateral absence of the vas deferens
- Congenital central hypoventilation syndrome
- Congenital contractural arachnodactyly
- Congenital diaphragmatic hernia
- Congenital dyserythropoietic anemia
- Congenital fiber type disproportion
- Congenital fibrosis of the extraocular muscles
- Congenital generalized lipodystrophy
- Congenital hepatic fibrosis
- Congenital hyperinsulinism
- Congenital hypothyroidism
- Congenital insensitivity to pain with anhidrosis
- Congenital insensitivity to pain
- Congenital mirror movement disorder
- Congenital myasthenic syndrome
- Congenital nephrotic syndrome
- Congenital stromal corneal dystrophy
- Constipation
- Copd
- Core binding factor acute myeloid leukemia
- Cornelia de lange syndrome
- Cosmetics
- Costeff syndrome
- Costello syndrome
- Cough
- Cowden syndrome
- Cpr
- Cranioectodermal dysplasia
- Craniofacial deafness hand syndrome
- Craniofacial microsomia
- Craniofrontonasal syndrome
- Craniometaphyseal dysplasia
- Creatine kinase
- Creatinine test
- Cri du chat syndrome
- Crigler najjar syndrome
- Crohn disease
- Croup
- Crouzon syndrome
- Cryopyrin associated periodic syndromes
- Cryptogenic cirrhosis
- Cryptosporidiosis
- Cushing disease
- Cutis laxa
- Cyclic neutropenia
- Cyclic vomiting syndrome
- Cystic fibrosis
- Cystinosis
- Cystinuria
- Cytochrome c oxidase deficiency
- Cytogenetically normal acute myeloid leukemia
- Czech dysplasia
D-E[edit | edit source]
Table of contents:
.A | .B | .C | .D | .E | .F | .G | .H | .I | .J | .K | .L | .M
.N | .O | .P | .Q | .R | .S | .T | .U | .V | .W | .X | .Y | .Z
- Danon disease
- Dari
- Darier disease
- Deafness and myopia syndrome
- Dehydration
- Delirium
- Dementia with lewy bodies
- Dementia
- Dengue
- Dent disease
- Dentatorubral pallidoluysian atrophy
- Dentinogenesis imperfecta
- Dentures
- Depression
- Dermatofibrosarcoma protuberans
- Desmoid tumor
- Desmosterolosis
- Diabetes
- Dialysis
- Diarrhea
- Diastrophic dysplasia
- Diets
- Differential diagnosis
- Dihydrolipoamide dehydrogenase deficiency
- Dihydropyrimidinase deficiency
- Dihydropyrimidine dehydrogenase deficiency
- Diphtheria
- Disabilities
- Disasters
- Dislocations
- Display
- Distal 18q deletion syndrome
- Donohue syndrome
- Dopamine beta hydroxylase deficiency
- Dopamine transporter deficiency syndrome
- Doppler ultrasound
- Down syndrome
- Drowning
- Drug testing
- Dupuytren contracture
- Dwarfism
- Dyskeratosis congenita
- Dystonia 16
- Dystonia
- Dystrophic epidermolysis bullosa
- Dzongkha
- Earthquakes
- Ebola
- Eczema
- Edema
- Ehlers danlos syndrome
- Elastography
- Electrocardiogram
- Emanuel syndrome
- Emery dreifuss muscular dystrophy
- Emphysema
- Encephalitis
- Encephalocraniocutaneous lipomatosis
- Endocarditis
- Endometriosis
- Endoscopy
- Epidermal nevus
- Epidermolysis bullosa simplex
- Epidermolytic hyperkeratosis
- Epilepsy
- Episodic ataxia
- Ergonomics
- Erythrokeratodermia variabilis et progressiva
- Erythromelalgia
- Essential pentosuria
- Essential thrombocythemia
- Essential tremor
- Ethylmalonic encephalopathy
- Ewing sarcoma
- Eyewear
F-H[edit | edit source]
Table of contents:
.A | .B | .C | .D | .E | .F | .G | .H | .I | .J | .K | .L | .M
.N | .O | .P | .Q | .R | .S | .T | .U | .V | .W | .X | .Y | .Z
- Fabry disease
- Facioscapulohumeral muscular dystrophy
- Factor v deficiency
- Factor v leiden thrombophilia
- Factor vii deficiency
- Factor x deficiency
- Factor xi deficiency
- Factor xiii deficiency
- Fainting
- Falls
- Familial adenomatous polyposis
- Familial atrial fibrillation
- Familial dilated cardiomyopathy
- Familial dysautonomia
- Familial encephalopathy with neuroserpin inclusion bodies
- Familial erythrocytosis
- Familial exudative vitreoretinopathy
- Familial focal epilepsy with variable foci
- Familial glucocorticoid deficiency
- Familial hemiplegic migraine
- Familial hemophagocytic lymphohistiocytosis
- Familial hyperaldosteronism
- Familial hypercholesterolemia
- Familial hypertrophic cardiomyopathy
- Familial hypobetalipoproteinemia
- Familial isolated hyperparathyroidism
- Familial lipoprotein lipase deficiency
- Familial mediterranean fever
- Familial osteochondritis dissecans
- Familial partial lipodystrophy
- Familial porencephaly
- Familial thoracic aortic aneurysm and dissection
- Fanconi anemia
- Farber lipogranulomatosis
- Farsightedness
- Fatigue
- Feingold syndrome
- Fever
- Fibrochondrogenesis
- Fibrodysplasia ossificans progressiva
- Fibromyalgia
- Fibronectin glomerulopathy
- Fish eye disease
- Fistulas
- Floods
- Flu
- Fluoroscopy
- Focal dermal hypoplasia
- Fractures
- Fragile x syndrome
- Fraser syndrome
- Frasier syndrome
- French
- Friedreich ataxia
- Frontometaphyseal dysplasia
- Frontonasal dysplasia
- Frostbite
- Fryns syndrome
- Fucosidosis
- Fukuyama congenital muscular dystrophy
- Fumarase deficiency
- Galactosemia
- Galactosialidosis
- Gallstones
- Gangrene
- Gas
- Gastroenteritis
- Gastrointestinal stromal tumor
- Gaucher disease
- Geleophysic dysplasia
- Generalized arterial calcification of infancy
- Generalized pustular psoriasis
- Genitopatellar syndrome
- German
- Gestational diabetes
- Ghosal hematodiaphyseal dysplasia
- Giant axonal neuropathy
- Gilbert syndrome
- Gillespie syndrome
- Gitelman syndrome
- Glanzmann thrombasthenia
- Glaucoma
- Globozoospermia
- Glucose 6 phosphate dehydrogenase deficiency
- Glucose phosphate isomerase deficiency
- Glutamate formiminotransferase deficiency
- Glutaric acidemia type I
- Glutathione synthetase deficiency
- Glycogen storage disease type 0
- Glycogen storage disease type I
- Glycogen storage disease type iii
- Glycogen storage disease type iv
- Glycogen storage disease type v
- Glycogen storage disease type vii
- Gonorrhea
- Gorlin syndrome
- Gout
- Gram stain
- Granulomatosis with polyangiitis
- Graves disease
- Gray platelet syndrome
- Greig cephalopolysyndactyly syndrome
- Griscelli syndrome
- Guanidinoacetate methyltransferase deficiency
- Guillain barre syndrome
- Gujarati
- Hailey hailey disease
- Hajdu cheney syndrome
- Hand foot genital syndrome
- Harlequin ichthyosis
- Hartnup disease
- Hashimoto thyroiditis
- Hayfever
- Head and neck squamous cell carcinoma
- Headache
- Heartburn
- Hematocrit test
- Hemochromatosis
- Hemoglobin electrophoresis
- Hemophilia
- Hemorrhoids
- Hennekam syndrome
- Hepatic lipase deficiency
- Hepatitis
- Hereditary angioedema
- Hereditary antithrombin deficiency
- Hereditary diffuse gastric cancer
- Hereditary folate malabsorption
- Hereditary fructose intolerance
- Hereditary hemochromatosis
- Hereditary hemorrhagic telangiectasia
- Hereditary hyperekplexia
- Hereditary leiomyomatosis and renal cell cancer
- Hereditary multiple osteochondromas
- Hereditary neuralgic amyotrophy
- Hereditary neuropathy with liability to pressure palsies
- Hereditary pancreatitis
- Hereditary spherocytosis
- Hereditary xanthinuria
- Hermansky pudlak syndrome
- Hernia
- Heroin
- Heterotaxy syndrome
- Hiccups
- Hidradenitis suppurativa
- Hindi
- Hirschsprung disease
- Histidinemia
- Histoplasmosis
- Hives
- Hmong
- Holocarboxylase synthetase deficiency
- Holt oram syndrome
- Homocystinuria
- Horizontal gaze palsy with progressive scoliosis
- Hormones
- Horner syndrome
- Huntington disease
- Hurricanes
- Hyaline fibromatosis syndrome
- Hydrocephalus
- Hyperglycemia
- Hyperkalemic periodic paralysis
- Hyperlysinemia
- Hypermethioninemia
- Hyperphosphatemic familial tumoral calcinosis
- Hyperprolinemia
- Hypertension
- Hyperthyroidism
- Hypochondrogenesis
- Hypochondroplasia
- Hypoglycemia
- Hypohidrotic ectodermal dysplasia
- Hypokalemic periodic paralysis
- Hypomagnesemia with secondary hypocalcemia
- Hypomyelination and congenital cataract
- Hypophosphatasia
- Hypothermia
- Hypothyroidism
- Hysterectomy
- Hysteroscopy
I-K[edit | edit source]
Table of contents:
.A | .B | .C | .D | .E | .F | .G | .H | .I | .J | .K | .L | .M
.N | .O | .P | .Q | .R | .S | .T | .U | .V | .W | .X | .Y | .Z
- Ichthyosis with confetti
- Idiopathic infantile hypercalcemia
- Idiopathic inflammatory myopathy
- Idiopathic pulmonary fibrosis
- Immune thrombocytopenia
- Impetigo
- Inclusion body myopathy 2
- Incontinentia pigmenti
- Indigestion
- Indonesian
- Infantile neuroaxonal dystrophy
- Infantile onset spinocerebellar ataxia
- Infections
- Infertility
- Inhalants
- Insomnia
- Intervertebral disc disease
- Intestinal pseudo obstruction
- Intrahepatic cholestasis of pregnancy
- Iron tests
- Iron
- Isolated congenital asplenia
- Isolated growth hormone deficiency
- Isolated hyperckemia
- Isovaleric acidemia
- Italian
- Itching
- Jacobsen syndrome
- Japanese
- Jaundice
- Joubert syndrome
- Junctional epidermolysis bullosa
- Juvenile idiopathic arthritis
- Juvenile myoclonic epilepsy
- Juvenile paget disease
- Juvenile polyposis syndrome
- Juvenile primary lateral sclerosis
- Kabuki syndrome
- Kallmann syndrome
- Karen
- Kaufman oculocerebrofacial syndrome
- Kawasaki disease
- Kearns sayre syndrome
- Keratoconus
- Keratoderma with woolly hair
- Khmer
- Kidney stones
- Kindler syndrome
- Kleefstra syndrome
- Klinefelter syndrome
- Kniest dysplasia
- Knobloch syndrome
- Korean
- Krabbe disease
- Kurdish
- Kuskokwim syndrome
L[edit | edit source]
- L1 syndrome
- Lab tests
- Lactate dehydrogenase deficiency
- Lactose intolerance
- Laing distal myopathy
- Lamellar ichthyosis
- Langer mesomelic dysplasia
- Langerhans cell histiocytosis
- Languages
- Lao
- Laparoscopy
- Laron syndrome
- Larsen syndrome
- Lateral meningocele syndrome
- Lattice corneal dystrophy type I
- Leber congenital amaurosis
- Leber hereditary optic neuropathy
- Left ventricular noncompaction
- Legius syndrome
- Leigh syndrome
- Leishmaniasis
- Leprosy
- Leptin receptor deficiency
- Lesch nyhan syndrome
- Leukemia
- Leukocyte adhesion deficiency type 1
- Leukodystrophies
- Leukoencephalopathy with thalamus and brainstem involvement and high lactate
- Leukoencephalopathy with vanishing white matter
- Leydig cell hypoplasia
- Li fraumeni syndrome
- Liddle syndrome
- Liebenberg syndrome
- Lipoid proteinosis
- Liver function tests
- Loeys dietz syndrome
- Lowe syndrome
- Lujan syndrome
- Lung cancer
- Lupus
- Lyme disease
- Lymphangioleiomyomatosis
- Lymphedema distichiasis syndrome
- Lymphedema
- Lymphoma
- Lynch syndrome
- Lysinuric protein intolerance
- Lysosomal acid lipase deficiency
M[edit | edit source]
Table of contents:
.A | .B | .C | .D | .E | .F | .G | .H | .I | .J | .K | .L | .M
.N | .O | .P | .Q | .R | .S | .T | .U | .V | .W | .X | .Y | .Z
- Macrozoospermia
- Maffucci syndrome
- Majeed syndrome
- Malaria
- Malay
- Malignant hyperthermia
- Malignant migrating partial seizures of infancy
- Malnutrition
- Mammography
- Mandibuloacral dysplasia
- Mandibulofacial dysostosis with microcephaly
- Maple syrup urine disease
- Marfan syndrome
- Marijuana
- Marshallese
- Mastectomy
- Maternally inherited diabetes and deafness
- Maturity onset diabetes of the young
- Mccune albright syndrome
- Measles
- Meckel syndrome
- Medicaid
- Medicare
- Medicines
- Meesmann corneal dystrophy
- Megacystis microcolon intestinal hypoperistalsis syndrome
- Megalencephalic leukoencephalopathy with subcortical cysts
- Meige disease
- Melanoma
- Melorheostosis
- Memory
- Men
- Meniere disease
- Meningitis
- Menkes syndrome
- Menopause
- Menstruation
- Mercury
- Mesothelioma
- Metachromatic leukodystrophy
- Metatropic dysplasia
- Methamphetamine
- Methylmalonic acidemia with homocystinuria
- Methylmalonic acidemia
- Mevalonate kinase deficiency
- Microphthalmia with linear skin defects syndrome
- Microphthalmia
- Microvillus inclusion disease
- Migraine
- Miller syndrome
- Milroy disease
- Minerals
- Miscarriage
- Mitochondrial complex I deficiency
- Mitochondrial trifunctional protein deficiency
- Miyoshi myopathy
- Moebius syndrome
- Moles
- Molybdenum cofactor deficiency
- Monilethrix
- Mosaic variegated aneuploidy syndrome
- Motion sickness
- Mowat wilson syndrome
- Moyamoya disease
- Mpox
- Mrsa
- Mucolipidosis iii gamma
- Mucolipidosis type iv
- Mucopolysaccharidosis type I
- Mucopolysaccharidosis type ii
- Mucopolysaccharidosis type iii
- Mucopolysaccharidosis type iv
- Mucopolysaccharidosis type vii
- Muenke syndrome
- Multiple endocrine neoplasia
- Multiple epiphyseal dysplasia
- Multiple myeloma
- Multiple pterygium syndrome
- Multiple sclerosis
- Multiple sulfatase deficiency
- Multiple system atrophy
- Mumps
- Myasthenia gravis
- Mycosis fungoides
- Myelography
- Myhre syndrome
- Myoclonic epilepsy with ragged red fibers
- Myofibrillar myopathy
- Myosin storage myopathy
- Myositis
- Myotonia congenita
- Myotonic dystrophy
N[edit | edit source]
- Nager syndrome
- Narcolepsy
- Nearsightedness
- Nemaline myopathy
- Nepali
- Nephrogenic diabetes insipidus
- Nephronophthisis
- Netherton syndrome
- Neuroblastoma
- Neuroferritinopathy
- Neurofibromatosis type 1
- Neurofibromatosis type 2
- Neurofibromatosis
- Neurological exam
- Neuromyelitis optica
- Neutral lipid storage disease with myopathy
- Nijmegen breakage syndrome
- Noise
- Non alcoholic fatty liver disease
- Nonbullous congenital ichthyosiform erythroderma
- Nonketotic hyperglycinemia
- Nonstress test
- Noonan syndrome with multiple lentigines
- Noonan syndrome
- Norrie disease
- Nutrition
O[edit | edit source]
- Obesity
- Obsessive compulsive disorder
- Obstructive sleep apnea
- Ochoa syndrome
- Ocular albinism
- Oculocutaneous albinism
- Oculodentodigital dysplasia
- Oculofaciocardiodental syndrome
- Oculopharyngeal muscular dystrophy
- Ollier disease
- Omenn syndrome
- Optic atrophy type 1
- Ornithine transcarbamylase deficiency
- Ornithine translocase deficiency
- Oromo
- Orthodontia
- Orthostatic hypotension
- Osteoarthritis
- Osteogenesis imperfecta
- Osteoglophonic dysplasia
- Osteonecrosis
- Osteopetrosis
- Osteoporosis pseudoglioma syndrome
- Osteoporosis
- Ostomy
- Otospondylomegaepiphyseal dysplasia
- Otulipenia
- Ovarian cancer
- Ozone
P[edit | edit source]
- Pachyonychia congenita
- Paget disease of bone
- Pain
- Pancreatitis
- Pap smear
- Paralysis
- Paramyotonia congenita
- Parathyroid cancer
- Parenting
- Parkinson disease
- Paroxysmal extreme pain disorder
- Paroxysmal nocturnal hemoglobinuria
- Partington syndrome
- Pearson syndrome
- Pelizaeus merzbacher disease
- Pemphigus
- Pendred syndrome
- Periventricular heterotopia
- Permanent neonatal diabetes mellitus
- Perrault syndrome
- Perry syndrome
- Persistent mullerian duct syndrome
- Pesticides
- Pet scan
- Peters anomaly
- Peters plus syndrome
- Peutz jeghers syndrome
- Pfeiffer syndrome
- Phenylketonuria
- Pheochromocytoma
- Phobias
- Phosphoglycerate kinase deficiency
- Phosphoglycerate mutase deficiency
- Phosphoribosylpyrophosphate synthetase superactivity
- Piebaldism
- Pilomatricoma
- Pinkeye
- Plague
- Pneumonia
- Pohnpeian
- Poikiloderma with neutropenia
- Poisoning
- Poland syndrome
- Polish
- Polycystic kidney disease
- Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
- Polycystic ovary syndrome
- Polycythemia vera
- Polymicrogyria
- Pompe disease
- Pontocerebellar hypoplasia
- Popliteal pterygium syndrome
- Porphyria
- Portuguese
- Potassium aggravated myotonia
- Potassium
- Potocki shaffer syndrome
- Prediabetes
- Preeclampsia
- Pregnancy test
- Pregnancy
- Prekallikrein deficiency
- Primary carnitine deficiency
- Primary ciliary dyskinesia
- Primary familial brain calcification
- Primary hyperoxaluria
- Primary myelofibrosis
- Primary sclerosing cholangitis
- Prion disease
- Progressive external ophthalmoplegia
- Progressive familial intrahepatic cholestasis
- Progressive osseous heteroplasia
- Progressive pseudorheumatoid dysplasia
- Progressive supranuclear palsy
- Prolidase deficiency
- Proopiomelanocortin deficiency
- Propionic acidemia
- Prostate cancer
- Protein c deficiency
- Protein s deficiency
- Proteus syndrome
- Prothrombin deficiency
- Pseudoachondroplasia
- Pseudocholinesterase deficiency
- Pseudohypoaldosteronism type 1
- Pseudohypoaldosteronism type 2
- Pseudoxanthoma elasticum
- Psoriasis
- Psoriatic arthritis
- Puberty
- Pulmonary alveolar microlithiasis
- Pulmonary arterial hypertension
- Pulmonary veno occlusive disease
- Pulse oximetry
- Punjabi
- Purine nucleoside phosphorylase deficiency
- Pyle disease
- Pyruvate carboxylase deficiency
- Pyruvate dehydrogenase deficiency
- Pyruvate kinase deficiency
R[edit | edit source]
- Rabies
- Radon
- Rapadilino syndrome
- Rapid onset dystonia parkinsonism
- Rashes
- Raynaud phenomenon
- Refsum disease
- Rehabilitation
- Renal coloboma syndrome
- Renal hypouricemia
- Renal tubular acidosis with deafness
- Renpenning syndrome
- Restless legs syndrome
- Reticulocyte count
- Retinal arterial macroaneurysm with supravalvular pulmonic stenosis
- Retinitis pigmentosa
- Retinoblastoma
- Retroperitoneal fibrosis
- Rett syndrome
- Rheumatoid arthritis
- Rhizomelic chondrodysplasia punctata
- Rickets
- Ring chromosome 14 syndrome
- Ring chromosome 20 syndrome
- Rippling muscle disease
- Roberts syndrome
- Robinow syndrome
- Romano ward syndrome
- Rosacea
- Rothmund thomson syndrome
- Rotor syndrome
- Rubella
- Rubinstein taybi syndrome
S[edit | edit source]
Table of contents:
.A | .B | .C | .D | .E | .F | .G | .H | .I | .J | .K | .L | .M
.N | .O | .P | .Q | .R | .S | .T | .U | .V | .W | .X | .Y | .Z
- Saethre chotzen syndrome
- Safety
- Samoan
- Sandhoff disease
- Sarcoidosis
- Scabies
- Scalp ear nipple syndrome
- Scars
- Schindler disease
- Schizoaffective disorder
- Schizophrenia
- Schwannomatosis
- Sciatica
- Scleroderma
- Scoliosis
- Seasonal affective disorder
- Seizures
- Semen analysis
- Sentinel lymph node biopsy
- Sepiapterin reductase deficiency
- Sepsis
- Serbian
- Severe congenital neutropenia
- Sezary syndrome
- Shingles
- Shock
- Shwachman diamond syndrome
- Sialic acid storage disease
- Sialidosis
- Sialuria
- Sick sinus syndrome
- Sickle cell disease
- Sinusitis
- Sitosterolemia
- Sjogren syndrome
- Skin biopsy
- Sleep study
- Smallpox
- Smith lemli opitz syndrome
- Smoking
- Snoring
- Sodium
- Somali
- Sonogram
- Sotos syndrome
- Spina bifida
- Spinal and bulbar muscular atrophy
- Spinal muscular atrophy with lower extremity predominance
- Spinal muscular atrophy with progressive myoclonic epilepsy
- Spinal muscular atrophy
- Spinocerebellar ataxia type 1
- Spinocerebellar ataxia type 6
- Spondylocarpotarsal synostosis syndrome
- Spondylocostal dysostosis
- Spondyloenchondrodysplasia with immune dysregulation
- Spondyloepiphyseal dysplasia congenita
- Spondyloperipheral dysplasia
- Spondylothoracic dysostosis
- Sporadic hemiplegic migraine
- Sputum culture
- Statins
- Steatocystoma multiplex
- Steroids
- Stickler syndrome
- Stillbirth
- Stormorken syndrome
- Stress
- Stroke
- Sturge weber syndrome
- Stuttering
- Subcortical band heterotopia
- Succinic semialdehyde dehydrogenase deficiency
- Sudden infant death syndrome
- Sudden infant death with dysgenesis of the testes syndrome
- Suicide
- Supravalvular aortic stenosis
- Surgery
- Swahili
- Sweat
- Swyer syndrome
- Symptoms
- Syphilis
- Syringomyelia
- Systemic lupus erythematosus
- Systemic mastocytosis
- Systemic scleroderma
T[edit | edit source]
- Tagalog
- Tangier disease
- Tanning
- Tarsal carpal coalition syndrome
- Tay sachs disease
- Tears
- Telehealth
- Tendinitis
- Tetanus
- Tetrahydrobiopterin deficiency
- Tetrasomy 18p
- Thai
- Thalassemia
- Thanatophoric dysplasia
- Therapeutic drug monitoring
- Thiamine responsive megaloblastic anemia syndrome
- Thrombocytopenia absent radius syndrome
- Thrombotic thrombocytopenic purpura
- Thyroglobulin
- Thyroid antibodies
- Tietz syndrome
- Timothy syndrome
- Tinnitus
- Tongan
- Tonsillitis
- Tornadoes
- Tourette syndrome
- Toxoplasmosis
- Transthyretin amyloidosis
- Treacher collins syndrome
- Tremor
- Trichohepatoenteric syndrome
- Trichomoniasis
- Trichorhinophalangeal syndrome type I
- Trichothiodystrophy
- Triglycerides
- Trimethylaminuria
- Triosephosphate isomerase deficiency
- Triple a syndrome
- Trisomy 13
- Trisomy 18
- Trisomy x
- Troyer syndrome
- Tsunamis
- Tuberculosis
- Tuberous sclerosis complex
- Tubular aggregate myopathy
- Tumor necrosis factor receptor associated periodic syndrome
- Turkish
- Turner syndrome
- Type 1 diabetes
- Type 2 diabetes
- Type a insulin resistance syndrome
- Tyrosine hydroxylase deficiency
- Tyrosinemia
U-V[edit | edit source]
- Ukrainian
- Ulcerative colitis
- Uncombable hair syndrome
- Urdu
- Urinalysis
- Usher syndrome
- Vaccines
- Vacterl association
- Vaginitis
- Van der woude syndrome
- Vasculitis
- Vasectomy
- Vibratory urticaria
- Vici syndrome
- Vietnamese
- Vitamine
- Vitamins
- Vitelliform macular dystrophy
- Vitiligo
- Vohwinkel syndrome
- Volcanoes
- Von hippel lindau syndrome
- Von willebrand disease
W[edit | edit source]
- Waardenburg syndrome
- Wagr syndrome
- Waldenstrom macroglobulinemia
- Warfarin resistance
- Warsaw breakage syndrome
- Warts
- Weaver syndrome
- Weill marchesani syndrome
- Werner syndrome
- Weyers acrofacial dysostosis
- White sponge nevus
- Wildfires
- Williams syndrome
- Wilms tumor
- Wilson disease
- Winchester syndrome
- Wiskott aldrich syndrome
- Wolff parkinson white syndrome
- Wolfram syndrome
- Women
X-Y[edit | edit source]
- X linked severe combined immunodeficiency
- X linked thrombocytopenia
- Xeroderma pigmentosum
- Y chromosome infertility
- Yao syndrome
- Yiddish
Table of contents:
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.N | .O | .P | .Q | .R | .S | .T | .U | .V | .W | .X | .Y | .Z
Z[edit | edit source]
Medicine portal[edit | edit source]
WikiMD's medicine portal includes;
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