Category:Metabolic disorders: Difference between revisions
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Subcategories
This category has the following 10 subcategories, out of 10 total.
A
- Acid–base disturbances (11 P)
- Albinism (5 P)
- Amyloidosis (18 P)
E
G
- Gout (9 P)
I
L
- Leukodystrophies (9 P)
O
S
Pages in category "Metabolic disorders"
The following 200 pages are in this category, out of 399 total.
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6
A
- ACADL
- ACADS
- ACADVL
- ACAT1
- Aceruloplasminemia
- Acid alpha-glucosidase
- ACSF3
- Acyl-CoA oxidase deficiency
- Adenine phosphoribosyltransferase deficiency
- Adenosine deaminase deficiency
- Adenosine monophosphate deaminase deficiency type 1
- Adenylosuccinate lyase deficiency
- AdipoRon
- African iron overload
- AGXT
- AKU
- Alcohol intolerance
- Alcoholic ketoacidosis
- Aldolase A deficiency
- Alkalosis
- Alkaptonuria
- Alpha-aminoadipic and alpha-ketoadipic aciduria
- Amino acid transport disorder
- Aminoaciduria
- Aminoacylase 1 deficiency
- Aminolevulinic acid dehydratase deficiency porphyria
- Android fat distribution
- Anticachexia
- Apolipoprotein B deficiency
- Aramchol
- Arginine:glycine amidinotransferase deficiency
- Argininemia
- Argininosuccinic aciduria
- Armenia
- ATC code A
- ATPAF2
- Atransferrinemia
B
C
- Carbamoyl phosphate synthetase I
- Carbamoyl phosphate synthetase I deficiency
- Carbonic anhydrase 12
- Carnitine palmitoyltransferase I deficiency
- Carnitine palmitoyltransferase II
- Carnitine palmitoyltransferase II deficiency
- Carnitine-acylcarnitine translocase
- Carnosinemia
- Cationic amino acid transporter 2
- CC-1088
- Centrifugal lipodystrophy
- Cerebral calcifications opalescent teeth phosphaturia
- Cerebral creatine deficiency
- Cerebrotendinous xanthomatosis
- Cherry-red spot
- Chondrocalcinosis
- Chylomicron retention disease
- Citrin
- Citrullinemia
- Citrullinemia type I
- Coenzyme Q10 deficiency
- Combined malonic and methylmalonic aciduria
- Congenital disorder of glycosylation
- Congenital disorders of amino acid metabolism
- Congenital lactic acidosis
- Contraction alkalosis
- Coproporphyrinogen I
- Coproporphyrinogen III
- Corneal crystals myopathy neuropathy
- Creatine transporter defect
- Crystalluria
- CTP synthetase
- Cystathioninuria
- Cystinosis
- Cytochrome b5 deficiency
D
- D-bifunctional protein deficiency
- D-Glyceric acidemia
- Dady
- DDOST-CDG (CDG-Ir)
- Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy
- Dicarboxylic aminoaciduria
- Diet-induced obesity model
- Diglyceride acyltransferase
- Dihydropyrimidinase
- Dihydropyrimidine dehydrogenase deficiency
- Dionisi–Vici–Sabetta–Gambarara syndrome
- Dolichol kinase deficiency
E
F
G
- Galactokinase deficiency
- Galactose epimerase deficiency
- Galactose-1-phosphate uridylyltransferase deficiency
- Galactosylceramidase
- Gangliosidosis
- Gasping syndrome
- GBR-13069
- Gentech Pharmaceutical
- Gierke
- Globel disaccharide intolerance
- Glucagon receptor family
- Glucose-galactose malabsorption
- Glutamate dehydrogenase
- Glutaminase deficiency
- Glutaric acid
- Glutaric acidemia type 2
- Glutaryl-CoA
- Glutathione synthetase deficiency
- Glycerol kinase deficiency
- Glycogen storage disease
- Glycogen storage disease type 0
- Glycogen storage disease type III
- Glycogen storage disease type IV
- Glycogen storage disease type IX
- Glycogen storage disease type V
- Glycogen storage disease type VI
- Glycoproteinosis
- Goldstein–Hutt syndrome
- GPR119
- Grass tetany
- GSD
- GT-45
- Guanidinoacetate methyltransferase deficiency
- Gunther disease
- GW-7647
H
- HAIR-AN syndrome
- Harderoporphyria
- Hartnup disease
- Hawkinsinuria
- HEC syndrome
- Hemochromatosis type 4
- Hepatic porphyria
- Hereditary haemochromatosis
- Hereditary hyperbilirubinemia
- Hershey bar
- Hexokinase deficiency
- Hi-wa itck
- High anion gap metabolic acidosis
- Histidinuria renal tubular defect syndrome
- HOGA1
- Holocarboxylase synthetase
- Holocarboxylase synthetase deficiency
- Homocarnosinase deficiency
- Homocitrulline
- Homocystine
- Homocystinuria due to MTHFR deficiency
- Horst Bickel
- HU6
- HUPRA syndrome
- Hurler
- Hurler syndrome
- Hyperaminoacidemia
- Hyperammonemia
- Hyperglycerolemia
