Disease #02228

Official abbreviation CORDX-1
Name dystrophy, cone-rod, X-linked, type 1 (CORDX-1)
OMIM ID 304020
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene RPGR
Associated tissues -
Disease features -
Remarks -