Disease #01543 (RP10 (retinitis pigmentosa, type 10 (RP10)), OMIM:180105)

Official abbreviation RP10
Name retinitis pigmentosa, type 10 (RP10)
OMIM ID 180105
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene IMPDH1
Associated tissues -
Disease features -
Remarks -

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