Congenital Stationary Night Blindness Autosomal Domit 1
Disease ID: disease_node_20051
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| Dbxref | MIM:610445 |
|---|---|
| Subclassof | DOID_0050534, DOID_0050736 |
| Data Source | DOID |
| Synonyms | CSNBAD1, rhodopsin-related congenital stationary night blindness |
| Doid Label | congenital stationary night blindness autosomal domit 1 |
| Doid Description | A congenital stationary night blindness characterized by autosomal domit inheritance that has_material_basis_in mutations in the RHO gene on chromosome 3q22.1. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_20051 |
| Doid Id | DOID_0110862 |
| Disease Has Basis In | HP_0001197 |
| Label | Congenital Stationary Night Blindness Autosomal Domit 1 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)