Charcot-Marie-Tooth Disease, Axonal Type 2W
Disease ID: disease_node_18858
Connections displayed (default: 10).
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| Dbxref | MIM:616625 |
|---|---|
| Subclassof | DOID_0050736, DOID_0050539 |
| Data Source | DOID |
| Synonyms | CMT2W, Charcot-Marie-Tooth neuropathy type 2W, autosomal dominant axonal Charcot-Marie-Tooth disease type 2W |
| Doid Label | Charcot-Marie-Tooth disease, axonal type 2W |
| Doid Description | A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the HARS gene on chromosome 5q31. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_18858 |
| Doid Id | DOID_0110162 |
| Label | Charcot-Marie-Tooth Disease, Axonal Type 2W |
- 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)