Disease #01261

Official abbreviation CORD-2
Name dystrophy, cone-rod, type 2 (CORD-2)
OMIM ID 120970
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene CRX
Associated tissues -
Disease features -
Remarks -