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Disease association ontology term - MONDO:0014256 - retinitis pigmentosa 67

Term summary

ID
MONDO:0014256
Name
retinitis pigmentosa 67
Ontology or CV name
Disease association
Definition
Any retinitis pigmentosa in which the cause of the disease is a mutation in the NEK2 gene.

Parents

Annotation

Disease association

MONDO:0014256 - retinitis pigmentosa 67

References:

Genes: