Charcot-Marie-Tooth Disease Type 3
Disease ID: disease_node_18838
Connections displayed (default: 10).
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| Dbxref | MIM:145900 |
|---|---|
| Subclassof | DOID_0050736, DOID_10595, DOID_0050737 |
| Data Source | DOID |
| Synonyms | DEJERINE-SOTTAS NEUROPATHY, DEJERINE-SOTTAS SYNDROME |
| Doid Label | Charcot-Marie-Tooth disease type 3 |
| Doid Description | A Charcot-Marie-Tooth disease that is characterized by motor and sensory peripheral neuropathies caused by demyelination. OMIM mapping confirmed by DO. [SN]. |
| Has Material Basis In | GENO_0000147, GENO_0000148 |
| Disease Node Id | disease_node_18838 |
| Doid Id | DOID_0050540 |
| Label | Charcot-Marie-Tooth Disease Type 3 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)