Disease #03285 (CSNB1C (blindness, night, stationary, congenital, type 1C (CSNB-1C)), OMIM:613216)
| Official abbreviation |
CSNB1C |
| Name |
blindness, night, stationary, congenital, type 1C (CSNB-1C) |
| OMIM ID |
613216 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
6 |
| Phenotype entries for this disease |
6 |
| Associated with 1 gene |
TRPM1 |
| 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
|