Congenital Nystagmus 1
Disease ID: disease_node_16615
Connections displayed (default: 10).
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| Dbxref | GARD:2969, MIM:310700 |
|---|---|
| Subclassof | DOID_9649, DOID_0050739 |
| Data Source | DOID |
| Synonyms | NYS1, X-linked infantile nystagmus 1, congenital motor nystagmus 1 |
| Doid Label | congenital nystagmus 1 |
| Doid Description | A congenital nystagmus that has_material_basis_in mutation in the FRMD7 gene on chromosome Xq26.2. |
| Has Material Basis In | GENO_0000934 |
| Disease Node Id | disease_node_16615 |
| Doid Id | DOID_0111790 |
| Disease Has Basis In | HP_0001197 |
| Label | Congenital Nystagmus 1 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Genetic Disease(ID:disease_node_15586) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Nystagmus, Congenital(ID:disease_node_10580) (Disease)