Disease #03505 (RP60 (retinitis pigmentosa, type 60 (RP60)), OMIM:613983)

Official abbreviation RP60
Name retinitis pigmentosa, type 60 (RP60)
OMIM ID 613983
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene PRPF6
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)

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