Disease #03365 (RP56 (retinitis pigmentosa, type 56 (RP56, maculopathy)), OMIM:613581)

Official abbreviation RP56
Name retinitis pigmentosa, type 56 (RP56, maculopathy)
OMIM ID 613581
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene IMPG2
Associated tissues -
Disease features -
Remarks -