Disease #06171 (CSNB1H (Night blindness, congenital stationary, type 1H), OMIM:617024)
Official abbreviation |
CSNB1H |
Name |
Night blindness, congenital stationary, type 1H |
OMIM ID |
617024 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
GNB3 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2021-12-10 23:20:41 +01:00 (CET) |
Date last edited |
N/A |
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