Category:Skin conditions resulting from errors in metabolism
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Skin conditions resulting from errors in metabolism are caused by enzymatic defects that lead to an accumulation or deficiency of various cellular components, including, but not limited to—amino acids, carbohydrates, and lipids.
Pages in category "Skin conditions resulting from errors in metabolism"
The following 125 pages are in this category, out of 125 total. This list may not reflect recent changes.
A
C
F
- Fabry disease
- Familial alpha-lipoprotein deficiency
- Familial amyloid polyneuropathy
- Familial Amyloidosis, Finnish Type
- Familial combined hyperlipidemia
- Familial defective apolipoprotein B-100
- Familial dysbetalipoproteinemia
- Familial hypertriglyceridemia
- Farber disease
- Fibrocytic dysmucopolysaccharidosis
- Fucosidosis
H
L
M
- Medication-induced hyperlipoproteinemia
- Milia-like calcinosis
- Mixed hepatic porphyria
- Mixed porphyria
- Mucopolysaccharidosis type I
- Mucopolysaccharidosis type I H-S
- Mucopolysaccharidosis type I S
- Mucopolysaccharidosis type IV
- Mucopolysaccharidosis type IX
- Mucopolysaccharidosis type VI
- Multiple-type hyperlipoproteinemia
- Myxedema