Disease #03436 (RP20 (retinitis pigmentosa, type 20 (RP20)), OMIM:613794)

Official abbreviation RP20
Name retinitis pigmentosa, type 20 (RP20)
OMIM ID 613794
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene RPE65
Associated tissues -
Disease features -
Remarks -