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peroxisomal disease

Disease Summary
Associated Targets (171)
Tbio

132

Tchem

24

Tdark

8

Tclin

7


Explore Associated Targets
Mondo Description 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.
Disease Ontology Description An inherited metabolic disorder that involves peroxisome malfunction.
Mondo Term and Equivalent IDs
MONDO:0019053:  peroxisomal disease
COHD:441268: 
ICD9:277.86: 
NCIT:C85005: 
Orphanet:68373: 
SCTID:238059005: 
UMLS:C0282528: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)