World Of Taxonomy
C85005Level 7

Peroxisomal Disorder

**Semantic type:** Disease or Syndrome

**Definition:** A group of congenital disorders of lipid metabolism, caused by loss of the normal peroxisomes. Signs and symptoms include developmental delays, mental retardation, facial abnormalities, hepatomegaly, and hypotonia.

**Synonyms:** - Disorder of Peroxisomal Function - Peroxisomal Function Disorder

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