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
GET
/api/v1/systems/nci_thesaurus/nodes/C85005Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.