Disease #05702 (RP87 (retinitis pigmentosa, type 87, choroidal involvement (RP87)), OMIM:618697)

Official abbreviation RP87
Name retinitis pigmentosa, type 87, choroidal involvement (RP87)
OMIM ID 618697
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene RPE65
Associated tissues -
Disease features -
Remarks -

  Powered by LOVD v.3.0 Build 29
LOVD software ©2004-2023 Leiden University Medical Center 		There are currently no updates.