Congenital Nystagmus 2
Disease ID: disease_node_20023
Connections displayed (default: 10).
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| Dbxref | GARD:9599, MIM:164100 |
|---|---|
| Subclassof | DOID_0050736, DOID_9649 |
| Data Source | DOID |
| Synonyms | NYS2, autosomal dominant congenital nystagmus 2, congenital motor nystagmus 2 |
| Doid Label | congenital nystagmus 2 |
| Doid Description | A congenital nystagmus that has_material_basis_in heterozygous mutation in a region of chromosome 6p12. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_20023 |
| Doid Id | DOID_0111792 |
| Disease Has Basis In | HP_0001197 |
| Label | Congenital Nystagmus 2 |
- Outgoing r'ship
SUBCLASS_OFto/from Nystagmus, Congenital(ID:disease_node_10580) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)