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 658 total.
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- 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
- ACADS
- ACADVL
- ACAT1
- ACSF3
- Acyl-CoA oxidase deficiency
- Acylcarnitine
- Adenosine monophosphate deaminase deficiency type 1
- Adenosine Monophosphate Deaminase Deficiency type 1
- Adenylosuccinate lyase
- Adenylosuccinate lyase deficiency
- Adipose tissue expandability hypothesis
- AGXT
- AKU
- Alcohol flush reaction
- Alcoholic ketoacidosis
- Aldolase A deficiency
- Alkalosis
- Alpha-aminoadipic and alpha-ketoadipic aciduria
- AMACR
- Amino acid transport disorder
- Aminoaciduria
- Aminoacylhistidine dipeptidase
- Aminoadipate-semialdehyde dehydrogenase
- Ammonia intoxication
- Amylo-1,6-glucosidase
- Android fat distribution
- Anticachexia
- Aramchol
- Arginine:glycine amidinotransferase deficiency
- Argininosuccinate lyase
- Argininosuccinic acidemia
- Arts syndrome
- Asian glow
- ATC code A
- ATPAF2
- Auto-brewery syndrome
B
- Beloranib
- Beta-galactosidase-1 deficiency
- Beta-ketothiolase
- Beta-ketothiolase deficiency
- Beta-Ureidoisobutyric acid
- BIBP-3226
- Bickel Fanconi glycogenosis
- Bile acid malabsorption
- Biopterin
- Biotinidase
- Branched-chain keto acid dehydrogenase kinase deficiency
- Bronze diabetes
- Butyrylcholinesterase deficiency
C
- Cachexy
- Calcium gout
- Calcium pyrophosphate dihydrate crystal deposition disease
- Calciuria
- Carbamoyl phosphate synthetase I
- Carbamoyl phosphate synthetase I deficiency
- Carbohydrate deficient glycoprotein syndrome
- Carbohydrate-insulin model
- Carbonic anhydrase 12
- Carbonic anhydrase II deficiency
- Cardiomyopathy hypogonadism metabolic anomalies
- Cardiovascular–kidney–metabolic syndrome
- Carnitine palmitoyltransferase I deficiency
- Carnitine palmitoyltransferase II
- Carnitine palmitoyltransferase II deficiency
- Carnitine-acylcarnitine translocase
- Carnosinase deficiency
- Cationic amino acid transporter 2
- 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
- Chanarin disease
- Cherry-red spot
- Cholestenol Delta-isomerase
- Cholesterol esterification disorder
- Chondrocalcinosis
- Citrin
- Citrullinemia
- 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
- 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's disease
- Corneal crystals myopathy neuropathy
- CPD-1
- CPPD
- CPS I
- Creatine transporter defect
- Crystalluria
- CTP synthetase
- Cystathionine beta synthetase deficiency
- Cystathionine beta-synthase
- Cystathioninuria
- Cystinuria-lysinuria
- Cytochrome b5 deficiency
D
- D-Glyceric acidemia
- DDOST-CDG (CDG-Ir)
- Defect in synthesis of adenosylcobalamin
- Dehydratase deficiency
- Delta-1-pyrroline-5-carboxylate dehydrogenase deficiency
- 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
- Dihydropyrimidinase
- Dihydropyrimidine dehydrogenase
- Dionisi–Vici–Sabetta–Gambarara syndrome
- Disorders of calcium metabolism
- DM
- Dolichol kinase deficiency
E
- Elafibranor
- Electrolyte imbalance
- Electron transfer flavoprotein, deficiency of
- Enolase deficiency type 1
- Enolase deficiency type 2
- Enolase deficiency type 3
- Enolase deficiency type 4
- Entero-oxyntin
- Epidemiology of metabolic syndrome
- Epimerase deficiency
- Equine metabolic syndrome
- Erythropoietic protoporphyria
- Essential fructosuria
- ETFDH
- Ethylmalonic aciduria
F
- Familial combined hyperlipidemia
- Familial hypertriglyceridemia
- Fanconi syndrome, renal, with nephrocalcinosis and renal stones
- Fatty acid oxidation inhibitors
- Fatty-acid metabolism disorder
- Ferrochelatase
- Fexaramine
- Finnish lethal neonatal metabolic syndrome
- FITM2
- Forbes' disease
- Forestier's disease
- Fructose bisphosphatase deficiency
- Fructose intolerance
- Fructose-bisphosphatase 2
- Fructosuria
- Fumaric aciduria
- Fumarylacetoacetic acid
