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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