" /> Retinitis pigmentosa 9 - CISMeF





Preferred Label : Retinitis pigmentosa 9;

Symbol : RP9;

CISMeF acronym : RP9;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the RP9 gene (RP9, 607331.0002);

Prefixed ID : #180104;

Details


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04/05/2025


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