Category:Metabolic disorders
From WikiMD's WELLNESSPEDIA
Subcategories
This category has the following 10 subcategories, out of 10 total.
Pages in category "Metabolic disorders"
The following 200 pages are in this category, out of 317 total.
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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
- 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
- Aramchol
- Arginine:glycine amidinotransferase deficiency
- Argininemia
- Argininosuccinic aciduria
- Armenia
- ATC code A
- 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
- Congenital disorder of glycosylation
- Congenital disorders of amino acid metabolism
- Congenital lactic acidosis
- Contraction alkalosis
- Coproporphyrinogen I
- Coproporphyrinogen III
- Crystalluria
- CTP synthetase
- Cystathioninuria
- Cystinosis
- Cytochrome b5 deficiency
D
E
F
G
- Galactokinase deficiency
- Galactose epimerase deficiency
- Galactose-1-phosphate uridylyltransferase deficiency
- Galactosylceramidase
- Gangliosidosis
- Gasping syndrome
- GBR-13069
- Gentech Pharmaceutical
- Glucose-galactose malabsorption
- 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
- GPR119
- Grass tetany
- 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
- Hexokinase deficiency
- High anion gap metabolic acidosis
- Holocarboxylase synthetase deficiency
- Homocarnosinase deficiency
- Homocystinuria due to MTHFR deficiency
- Horst Bickel
- HUPRA syndrome
- Hurler syndrome
- Hyperaminoacidemia
- Hyperammonemia
- Hyperglycerolemia
- Hyperhomocysteinemia
- Hyperinsulinemia
- Hyperinsulinemic hypoglycemia
- Hyperinsulinism
- Hyperinsulinism-hyperammonemia syndrome
- Hyperlysinemia
- Hypermetabolism
- Hypermethioninemia
- Hyperparathyroidism
- Hyperphenylalaninemia
- Hypertriglyceridemia
- Hypertryptophanemia
- Hypervalinemia
- Hyperventilation
- Hypoalphalipoproteinemia
- Hypocholesterolemia
- Hypomagnesemia with secondary hypocalcemia
- Hypothyroidism
- Hypouricemia
I
- I-cell disease
- Idazoxan
- Idiopathic hypoglycemia
- Idiopathic postprandial syndrome
- Iduronidase
- Iminoglycinuria
- Impaired fasting glucose
- Inborn error of lipid metabolism
- Inborn errors of carbohydrate metabolism
- Inborn errors of steroid metabolism
- Infantile Refsum disease
- Inherited disorders of trafficking
- IONIS-GCCRRx
- Iron metabolism disorder
- Isovaleric acid
