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Disease association ontology term - MONDO:0100268 - peroxisome biogenesis disorder due to PEX14 defect

Term summary

ID
MONDO:0100268
Name
peroxisome biogenesis disorder due to PEX14 defect
Ontology or CV name
Disease association
Definition
Any Zellweger spectrum disorder in which the cause of the disease is a mutation in the PEX14 gene.

Parents

Annotation

Disease association

MONDO:0013952 - peroxisome biogenesis disorder 13A (Zellweger)

References:

Genes: