Charcot-Marie-Tooth Disease Type 4G
Disease ID: disease_node_18828
Connections displayed (default: 10).
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| Dbxref | ICD10CM:G60.0, MIM:605285, ORDO:99953 |
|---|---|
| Subclassof | DOID_0050737, DOID_0050541 |
| Data Source | DOID |
| Synonyms | CMT4G, Charcot-Marie-Tooth neuropathy type 4G, HMSNR, autosomal recessive Charcot-Marie-Tooth disease type 4G, hereditary motor and sensory neuropathy Russe type |
| Doid Label | Charcot-Marie-Tooth disease type 4G |
| Doid Description | A Charcot-Marie-Tooth disease type 4 that has_material_basis_in homozygous mutation in the HK1 gene on chromosome 10q22. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_18828 |
| Doid Id | DOID_0110196 |
| Label | Charcot-Marie-Tooth Disease Type 4G |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Charcot-Marie-Tooth Disease Type 4(ID:disease_node_18827) (Disease)