Cone-rod dystrophy 2
Cone-rod dystrophy 2
Definition
Any cone-rod dystrophy in which the cause of the disease is a mutation in the CRX gene.
Also known as cone-rod dystrophy 2, cone-rod dystrophy caused by mutation in CRX, cone-rod dystrophy type 2, cone-rod retinal dystrophy-2, CORD2, CRD2, CRX cone-rod dystrophy, RCRD2 — per MONDO
Also identified as
- DOID 0111005 per MONDO
- ICD9 362.75 per MONDO
- NCIT C162399 per MONDO
- OMIM 120970 per MONDO
- SCTID 80328002 per MONDO
- UMLS C3489532 per MONDO
Affected Organs
| Organ | Involvement | Source |
|---|---|---|
| Camera-type eye | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Camera-type eye | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Retina | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Retina | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |