peroxisome biogenesis disorder due to PEX13 defect

http://purl.obolibrary.org/obo/MONDO_0100267

Any Zellweger spectrum disorder in which the cause of the disease is a mutation in the PEX13 gene. [ MONDO:patterns/disease_series_by_gene ]

Subsets

disease_grouping

IAO 0000233

https://github.com/monarch-initiative/mondo/issues/2632

created by

https://orcid.org/0000-0001-5208-3432

definition

Any Zellweger spectrum disorder in which the cause of the disease is a mutation in the PEX13 gene.

has exact synonym

peroxisome biogenesis disorder due to PEX13 defect, PEX13 related Zellweger spectrum disorder

MONDO:0100267

Subclass of: