Disease #03329 (CSNBO2 (Oguchi disease 2 (night blindness, stationary, congenitial, Oguchi type 1 (CSNBO-2))), OMIM:613411)
| Official abbreviation |
CSNBO2 |
| Name |
Oguchi disease 2 (night blindness, stationary, congenitial, Oguchi type 1 (CSNBO-2)) |
| OMIM ID |
613411 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
GRK1 |
| 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
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