Optic Atrophy 8
Disease ID: disease_node_17291
Connections displayed (default: 10).
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| Dbxref | MIM:616648 |
|---|---|
| Subclassof | DOID_0050736, DOID_5723 |
| Data Source | DOID |
| Synonyms | OPA8 |
| Doid Label | optic atrophy 8 |
| Doid Description | An optic atrophy characterized by progressive visual loss during the first or second decade of life that has_material_basis_in heterozygous mutation in a region on chromosome 16q21-q22. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_17291 |
| Doid Id | DOID_0111439 |
| Label | Optic Atrophy 8 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Optic Atrophy(ID:disease_node_5715) (Disease)