Disease association ontology term - MONDO:0013950 - peroxisome biogenesis disorder 11B

Term summary

ID: MONDO:0013950
Name: peroxisome biogenesis disorder 11B
Ontology or CV name: Disease association

Parents

is_a peroxisome biogenesis disorder due to PEX13 defect

Annotation

Disease association

MONDO:0013950 - peroxisome biogenesis disorder 11B

References:

PB_REF:0000006

Genes:

pex13 (SPAC3C7.10)