Category:Metabolic disorders
From WikiMD's WELLNESSPEDIA
Subcategories
This category has the following 10 subcategories, out of 10 total.
A
- Acid–base disturbances (11 P)
- Albinism (3 P)
- Amyloidosis (13 P)
E
G
- Gout (7 P)
I
L
- Leukodystrophies (8 P)
O
S
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
