|
| General Information | |||
|---|---|---|---|
| Term | congenital nystagmus 6 | ID (Ontology) | DOID:0111795 (Human Disease) |
| Definition | A congenital nystagmus that has_material_basis_in hemizygous of homoxygous mutation in the GPR143 gene on chromosome Xp22.2. | ||
| Also Known As | "NYS6" ; "X-linked congenital nystagmus 6" | ||
| Comment | |||
| Links to External Ontologies | |||
| DO.org | |||
| Annotations | |||
| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
|
|||
|
No relevant statements available
|
|||
|
||||||
physical disorder_____ pathologic nystagmus__| congenital nystagmus |__congenital nystagmus 6 |
| Spanning Tree View Settings | |||
|---|---|---|---|
| Parents/Children View Depth |
|||
Relationships
|
|||
| Is a | congenital nystagmus | ||
| Part of | |||
|
Synonyms & Secondary IDs
|
|||
| Synonyms | |||
|
|||
| Secondary IDs | |||
|
|
|||
|
External Crossreferences & Linkouts
|
|||
| MIM:300814 | |||