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
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