Congenital Stationary Night Blindness Autosomal Domit 3
Disease ID: disease_node_20052
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| Dbxref | MIM:610444 |
|---|---|
| Subclassof | DOID_0050534, DOID_0050736 |
| Data Source | DOID |
| Synonyms | CSNBAD3, Nougaret type congenital stationary night blindness |
| Doid Label | congenital stationary night blindness autosomal domit 3 |
| Doid Description | A congenital stationary night blindness characterized by autosomal domit inheritance that has_material_basis_in heterozygous mutation in the GNAT1 gene on chromosome 3p21. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_20052 |
| Doid Id | DOID_0110715 |
| Disease Has Basis In | HP_0001197 |
| Label | Congenital Stationary Night Blindness Autosomal Domit 3 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)