Disease #03680 (CSNB1E (blindness, night, stationary, congenital, type 1E (CSNB1E)), OMIM:614565)
| Official abbreviation |
CSNB1E |
| Name |
blindness, night, stationary, congenital, type 1E (CSNB1E) |
| OMIM ID |
614565 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
GPR179 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2020-11-22 21:14:33 +01:00 (CET) |
Individuals
|