Disease #02361 (RP18 (retinitis pigmentosa, type 18 (RP18)), OMIM:601414)

Official abbreviation RP18
Name retinitis pigmentosa, type 18 (RP18)
OMIM ID 601414
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene PRPF3
Associated tissues -
Disease features -
Remarks -