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Disease association ontology term - MONDO:0013611 - retinitis pigmentosa 62

Term summary

ID
MONDO:0013611
Name
retinitis pigmentosa 62
Ontology or CV name
Disease association
Definition
Any retinitis pigmentosa in which the cause of the disease is a mutation in the MAK gene.

Parents

Annotation

Disease association

MONDO:0013611 - retinitis pigmentosa 62

References:

Genes: