Disease #07115 (CORD14 (cone-rod dystrophy, type 14), OMIM:620342)
| Official abbreviation |
CORD14 |
| Name |
cone-rod dystrophy, type 14 |
| OMIM ID |
620342 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
UNC119 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2024-11-11 21:35:31 +01:00 (CET) |
| Date last edited |
N/A |
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