U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

CORD1 cone rod dystrophy 1 (autosomal dominant) [ Homo sapiens (human) ]

Gene ID: 1319, updated on 31-Aug-2024

Summary

Go to the top of the page Help
Official Symbol
CORD1provided by HGNC
Official Full Name
cone rod dystrophy 1 (autosomal dominant)provided by HGNC
Primary source
MIM:600624
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
CORD; CRD1

Genomic context

Go to the top of the page Help
Location:
18q21.1-q21.3

Bibliography

Go to the top of the pageHelp

Related articles in PubMed

  1. Deletion mapping of a retinal cone-rod dystrophy: assignment to 18q211. Warburg M, et al. Am J Med Genet, 1991 Jun 1. PMID 1867279

GeneRIFs: Gene References Into Functions

Phenotypes

Go to the top of the page Help

Associated conditions

Description Tests
cone rod dystrophy 1 (autosomal dominant)
OMIM: 600624GeneReviews: Not available

General gene information

Go to the top of the page Help

Property

  • phenotype only

Gene LinkOut

The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.

Molecular Biology Databases
Research Materials