Category:Metabolic disorders
From WikiMD.com Medical 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 10 subcategories, out of 10 total.
A
E
G
I
L
O
S
Pages in category "Metabolic disorders"
The following 200 pages are in this category, out of 636 total.
(previous page) (next page)2
3
- 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-Hydroxyisobutyryl-CoA deacylase deficiency
- 3-methyl glutaconic aciduria
- 3-Methylcrotonyl-CoA carboxylase deficiency
- 3-methylglutaconic acid
- 3-Methylglutaconic acid
- 3-Methylglutaconic aciduria
- 3-Methylglutaconyl-CoA
6
A
- ACADL
- ACADM deficiency
- ACADS
- ACADVL
- ACAT1
- Acid alpha-glucosidase
- ACSF3
- Acyl-CoA dehydrogenase, medium chain, deficiency of
- Acyl-CoA dehydrogenase, short chain, deficiency of
- Acyl-CoA oxidase deficiency
- Acylcarnitine
- Adenosine Monophosphate Deaminase Deficiency type 1
- Adenosine monophosphate deaminase deficiency type 1
- Adenylosuccinate lyase deficiency
- AdipoRon
- African iron overload
- AGAT deficiency
- AGXT
- AKU
- Alactasia
- Alcaptonuria
- Alcohol intolerance
- Alcoholic ketoacidosis
- ALDH3A2
- Aldolase A deficiency
- Alkalosis
- AMACR
- Amino acid transport disorder
- Aminoaciduria
- Aminoacylase 1 deficiency
- Ammonia intoxication
- Amylo-1,6-glucosidase
- Android fat distribution
- Anticachexia
- Apolipoprotein C-II deficiency
- APRT deficiency
- Aramchol
- ARG1 deficiency
- Arginine:glycine amidinotransferase deficiency
- Argininemia
- Argininosuccinic acidemia
- Argininosuccinic aciduria
- Armenia
- ASL deficiency
- ATC code A
- ATPAF2
- Atransferrinemia
B
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
- 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
- Centrifugal lipodystrophy
- Cerebral calcifications opalescent teeth phosphaturia
- Cerebral creatine deficiency
- Chanarin disease
- Cherry-red spot
- Cholestanol
- Chondrocalcinosis
- Citrin
- Citrullinemia
- Citrullinemia type I
- Citrullinuria
- Classic galactosemia
- Coenzyme Q10 deficiency
- Combined malonic and methylmalonic aciduria
- 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
- Coproporphyrinogen I
- Coproporphyrinogen III
- Cori disease
- Cori's disease
- Corneal crystals myopathy neuropathy
- CPPD
- 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)
- Dehydratase deficiency
- Deregulated
- Diabetes
- Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy
- Dibasic aminoaciduria type 1
- Dicarboxylic aminoaciduria
- Diet-induced obesity model
- Diglyceride acyltransferase
- Dihydropyrimidinase
- Dihydropyrimidine dehydrogenase
- Dionisi Vici Sabetta Gambarara syndrome
- Dionisi–Vici–Sabetta–Gambarara syndrome
- Dolichol kinase deficiency
E
- Elafibranor
- Electrolyte imbalance
- Electron transfer flavoprotein, deficiency of
- Enolase deficiency type 1
- Enolase deficiency type 3
- Entero-oxyntin
- Epidemiology of metabolic syndrome
- Epimerase deficiency
- Equine metabolic syndrome
- Ersofermin
- Erythropoietic protoporphyria
- Essential fructosuria
- ETFDH
- Ethylmalonic aciduria
- Ethylmalonic adipic aciduria
- Ethylmalonic-adipicaciduria
