Category:Metabolic disorders
From WikiMD's Wellness Encyclopedia
 | This category reflects the organization of International Statistical Classification of Diseases and Related Health Problems, 10th Revision. Generally, diseases outlined within the ICD-10 codes E70-E90 should be included in this category. |
Subcategories
This category has the following 7 subcategories, out of 7 total.
A
G
I
O
S
Pages in category "Metabolic disorders"
The following 200 pages are in this category, out of 813 total.
(previous page) (next page)1
2
3
- 3 alpha methylcrotonyl-Coa carboxylase 1 deficiency
- 3 alpha methylcrotonyl-coa carboxylase 2 deficiency
- 3 hydroxyisobutyric aciduria
- 3 methylglutaconyl coa hydratase deficiency
- 3-hydroxyacyl-coa dehydrogenase deficiency
- 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
- 3-methyl glutaconic aciduria
- 3-Methylglutaconic acid
- 3-methylglutaconic acid
- 3-Methylglutaconic aciduria
- 3-Methylglutaconyl-CoA
4
6
A
- ACADL
- ACADM deficiency
- ACADS
- ACADVL
- ACAT1
- Acid alpha-glucosidase
- Acquired partial lipodystrophy
- ACSF3
- Acyl-CoA dehydrogenase, medium chain, deficiency of
- Acyl-CoA dehydrogenase, short chain, deficiency of
- Acyl-CoA oxidase deficiency
- Acylcarnitine
- Adenosine monophosphate deaminase deficiency
- Adenosine monophosphate deaminase deficiency type 1
- Adenosine Monophosphate Deaminase Deficiency type 1
- Adenylosuccinase
- Adenylosuccinate lyase
- Adenylosuccinate lyase deficiency
- Adipose tissue expandability hypothesis
- AGAT deficiency
- AGXT
- AKU
- Alactasia
- Albert Niemann (pediatrician)
- Alcaptonuria
- Alcohol flush reaction
- Alcoholic ketoacidosis
- ALDH3A2
- Aldolase A deficiency
- Alkalosis
- Alkyldihydroxyacetonephosphate synthase deficiency
- Alpha-aminoadipic and alpha-ketoadipic aciduria
- AMACR
- Amino acid transport disorder
- Aminoaciduria
- Aminoacylase 1 deficiency
- Aminoacylhistidine dipeptidase
- Aminoadipate-semialdehyde dehydrogenase
- Ammonia intoxication
- Amylo-1,6-glucosidase
- Android fat distribution
- Anticachexia
- Apolipoprotein C-II deficiency
- APRT deficiency
- Aramchol
- ARG1 deficiency
- Arginine:glycine amidinotransferase deficiency
- Argininosuccinate lyase
- Argininosuccinic acidemia
- Arts syndrome
- Asian glow
- ASL deficiency
- ATC code A
- ATPAF2
- Atransferrinemia
B
- B-mannosidase deficiency
- BCKDHA
- BCKDHB
- Beloranib
- Beta-galactosidase-1 deficiency
- Beta-ketothiolase
- Beta-ketothiolase deficiency
- Beta-Ureidoisobutyric acid
- Bgd
- BH4 deficiency
- BIBP-3226
- Bickel Fanconi glycogenosis
- Bile acid malabsorption
- Bile acid synthesis disorders
- Biopterin
- Biotinidase
- Branched-chain keto acid dehydrogenase kinase deficiency
- Bronze diabetes
- Butyrylcholinesterase deficiency
C
- Cachectic
- Cachexy
- Calcium gout
- Calcium pyrophosphate dihydrate crystal deposition disease
- Calciuria
- Camptodactyly taurinuria
- Carbamoyl phosphate synthetase deficiency
- Carbamoyl phosphate synthetase I
- Carbamoyl phosphate synthetase I deficiency
- Carbohydrate deficient glycoprotein syndrome
- Carbohydrate-deficient glycoprotein syndrome
- Carbohydrate-insulin model
- Carbonic anhydrase 12
- Carbonic anhydrase II deficiency
- Cardiomyopathy hypogonadism metabolic anomalies
- Cardiovascular–kidney–metabolic syndrome
- Carnitine acylcarnitine translocase deficiency
- Carnitine palmitoyltransferase i deficiency
- Carnitine palmitoyltransferase I deficiency
- Carnitine palmitoyltransferase II
- Carnitine palmitoyltransferase II deficiency
- Carnitine uptake deficiency
- Carnitine-acylcarnitine translocase
- Carnosinase deficiency
- Cationic amino acid transporter 2
- CBS deficiency
- CC-1088
- CDG syndrome type 1A
- CDG syndrome type 1C
- CDG syndrome type 2
- CDG syndrome type 3
- CDG syndrome type 4
- Cerebral calcifications opalescent teeth phosphaturia
- Cerebral creatine deficiency
- Chanarin disease
- Cherry-red spot
- Cholestanol
- Cholestenol Delta-isomerase
- Cholesterol esterification disorder
- Chondrocalcinosis
- Citrin
- Citrullinemia
- Citrullinuria
- Classic galactosemia
- Combined malonic and methylmalonic aciduria
- Complex 1 mitochondrial respiratory chain deficiency
- Complex 2 mitochondrial respiratory chain deficiency
- Complex 3 mitochondrial respiratory chain deficiency
- Complex 4 mitochondrial respiratory chain deficiency
- Complex 5 mitochondrial respiratory chain deficiency
- Complex carbohydrate intolerance
- Congenital betalipoprotein deficiency syndrome
- Congenital disorder of glycosylation
- Congenital disorders of amino acid metabolism
- Congenital hepatic porphyria
- Congenital lactic acidosis
- Contraction alkalosis
- Copper deficiency familial benign
- Coproporphyrinogen I
- Coproporphyrinogen III
- Coproporphyrinogen III oxidase
- Cori disease
- Cori's disease
- Corneal crystals myopathy neuropathy
- CPD-1
- CPPD
- CPS I
- Creatine deficiency
- Creatine transporter defect
- Crystalluria
- CTP synthetase
- Cystathionine beta synthetase deficiency
- Cystathionine beta-synthase
- Cystathioninuria
- Cystin transport, protein defect of
- Cystine diathesis
- Cystine disease
- Cystinosis
- Cystinuria-lysinuria
- Cytochrome b5 deficiency
D
- D-Glyceric acidemia
- Dady
- DDOST-CDG (CDG-Ir)
- Defect in synthesis of adenosylcobalamin
- Dehydratase deficiency
- Delta-1-pyrroline-5-carboxylate dehydrogenase deficiency
- Deoxysphingolipid
- Deregulated
- DHTKD1
- Diabetes
- Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy
- Diacylglycerol O-acyltransferase 2
- Dibasic aminoaciduria type 1
- Dicarboxylic aminoaciduria
- Diet-induced obesity model
- Diglyceride acyltransferase
- Dihydrofolate reductase deficiency
