Optic Atrophy 10
Disease ID: disease_node_17293
Connections displayed (default: 10).
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| Dbxref | MIM:616732 |
|---|---|
| Subclassof | DOID_0050736, DOID_5723 |
| Data Source | DOID |
| Synonyms | OPA10, optic atrophy 10 with or without ataxia, mental retardation, and seizures |
| Doid Label | optic atrophy 10 |
| Doid Description | An optic atrophy characterized by early-onset optic neuropathy and mitochondrial defects that has_material_basis_in homozygous or compound heterozygous mutation in the RTN4IP1 gene on chromosome 6q21. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_17293 |
| Doid Id | DOID_0111434 |
| Label | Optic Atrophy 10 |
- 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)