Congenital Stationary Night Blindness 1A
Disease ID: disease_node_20044
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| Dbxref | MIM:310500 |
|---|---|
| Subclassof | DOID_0050534, DOID_0080012 |
| Data Source | DOID |
| Synonyms | CSNB1A, NBMI, complete CSNB X-linked, congenital stationary night blindness 1A X-linked, congenital stationary night blindness with myopia, hemeralopia-myopia, myopia-night blindness |
| Doid Label | congenital stationary night blindness 1A |
| Doid Description | A congenital stationary night blindness that has_material_basis_in mutation in the NYX gene on chromosome Xp11.4. |
| Has Material Basis In | GENO_0000149 |
| Disease Node Id | disease_node_20044 |
| Doid Id | DOID_0110870 |
| Disease Has Basis In | HP_0001197 |
| Label | Congenital Stationary Night Blindness 1A |
- Outgoing r'ship
SUBCLASS_OFto/from X-Linked Recessive Disease(ID:disease_node_13254) (Disease)