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Disease association ontology term - MONDO:0015013 - retinitis pigmentosa 77

Term summary

ID
MONDO:0015013
Name
retinitis pigmentosa 77
Ontology or CV name
Disease association
Definition
Any retinitis pigmentosa in which the cause of the disease is a mutation in the REEP6 gene.

Parents

Annotation

Disease association

MONDO:0015013 - retinitis pigmentosa 77

References:

Genes: