Format

Send to:

Choose Destination

CORD5 cone rod dystrophy 5 [ Homo sapiens (human) ]

Gene ID: 1322, discontinued on 12-May-2006
Official Symbol
CORD5provided by HGNC
Official Full Name
cone rod dystrophy 5provided by HGNC
Primary source
HGNC:HGNC:2248
See related
MIM:600977
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

GeneRIFs: Gene References Into FunctionsWhat's a GeneRIF?

Associated conditions

Description Tests
cone rod dystrophy 5
GeneReviews: Not available
Support Center