Disease #06963 (RP91 (retinitis pigmentosa, type 91), OMIM:153870)

Official abbreviation RP91
Name retinitis pigmentosa, type 91
OMIM ID 153870
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene IMPG1
Associated tissues -
Disease features -
Remarks -

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