Disease #04528

Official abbreviation RDGCA
Name dystrophy, retinal?, with inner retinal dysfunction and ganglion cell abnormalities (RDGCA)
OMIM ID 616079
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene ITM2B
Associated tissues -
Disease features -
Remarks -