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Disease association ontology term - MONDO:0100272 - peroxisome biogenesis disorder due to PEX7 defect

Term summary

ID
MONDO:0100272
Name
peroxisome biogenesis disorder due to PEX7 defect
Ontology or CV name
Disease association
Definition
Any peroxisome biogenesis disorder in which the cause of the disease is a mutation in the PEX7 gene.

Parents

Annotation

Disease association

MONDO:0008972 - rhizomelic chondrodysplasia punctata type 1

References:

Genes: