Disease #02140 (CSNB2A (blindness, night, stationary, congenital, type 2A (CSNB-2A)), OMIM:300071)
| Official abbreviation |
CSNB2A |
| Name |
blindness, night, stationary, congenital, type 2A (CSNB-2A) |
| OMIM ID |
300071 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
X-linked |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
CACNA1F |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|