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Disease association ontology term - MONDO:0100263 - peroxisome biogenesis disorder due to PEX6 defect

Term summary

ID
MONDO:0100263
Name
peroxisome biogenesis disorder due to PEX6 defect
Ontology or CV name
Disease association
Definition
Any Zellweger spectrum disorder in which the cause of the disease is a mutation in the PEX6 gene.

Parents

Annotation

Disease association

MONDO:0100263 - peroxisome biogenesis disorder due to PEX6 defect

References:

Genes:

MONDO:0013930 - peroxisome biogenesis disorder 4A (Zellweger)

References:

Genes:

MONDO:0013931 - peroxisome biogenesis disorder 4B

References:

Genes: