Optic Atrophy 12
Disease ID: disease_node_17294
Connections displayed (default: 10).
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| Dbxref | MIM:618977 |
|---|---|
| Subclassof | DOID_0050736, DOID_5723 |
| Data Source | DOID |
| Doid Label | optic atrophy 12 |
| Doid Description | An optic atrophy that is characterized by slowly progressive visual impairment with onset usually in the first decade and that has_material_basis_in heterozygous mutation in the AFG3L2 gene on chromosome 18p11. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_17294 |
| Doid Id | DOID_0080840 |
| Label | Optic Atrophy 12 |
- Outgoing r'ship
SUBCLASS_OFto/from Optic Atrophy(ID:disease_node_5715) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)