Charcot-Marie-Tooth Disease Axonal Type 2O
Disease ID: disease_node_18846
Connections displayed (default: 10).
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| Dbxref | ICD10CM:G60.0, MIM:614228, ORDO:284232 |
|---|---|
| Subclassof | DOID_0050736, DOID_0050539 |
| Data Source | DOID |
| Synonyms | Charcot-Marie-Tooth neuropathy axonal type 2O, autosomal dominant Charcot-Marie-Tooth disease type 2O, autosomal dominant axonal Charcot-Marie-Tooth disease type 2O |
| Doid Label | Charcot-Marie-Tooth disease axonal type 2O |
| Doid Description | A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the DYNC1H1 gene on chromosome 14q32. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_18846 |
| Doid Id | DOID_0110175 |
| Label | Charcot-Marie-Tooth Disease Axonal Type 2O |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Charcot-Marie-Tooth Disease Type 2(ID:disease_node_18839) (Disease)