Disease #04452 (CORD-21 (dystrophy, cone-rod, type 21 (CORD-21)), OMIM:616502)

Official abbreviation CORD-21
Name dystrophy, cone-rod, type 21 (CORD-21)
OMIM ID 616502
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene DRAM2
Associated tissues -
Disease features -
Remarks -