Disease #03472

Official abbreviation RP-38
Name retinitis pigmentosa, type 38 (RP-38)
OMIM ID 613862
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene MERTK
Associated tissues -
Disease features autosomal recessive
Remarks -