Charcot-Marie-Tooth Disease Type 1B
Disease ID: disease_node_18870
Connections displayed (default: 10).
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| Dbxref | ICD10CM:G60.0, MIM:118200, ORDO:101082 |
|---|---|
| Subclassof | DOID_0050736, DOID_0050538 |
| Data Source | DOID |
| Synonyms | CMT1B, Charcot-Marie-Tooth disease slow nerve conduction type linked to Duffy, Charcot-Marie-Tooth neuropathy type 1B, HMSN IB, HMSN1B, autosomal dominant Charcot-Marie-Tooth disease with focally folded myelin sheaths type 1B, hereditary motor and sensory neuropathy IB, peroneal muscular atrophy |
| Doid Label | Charcot-Marie-Tooth disease type 1B |
| Doid Description | A Charcot-Marie-Tooth disease type 1 that has_material_basis_in heterozygous mutation in the gene encoding myelin protein zero (MPZ). |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_18870 |
| Doid Id | DOID_0110152 |
| Label | Charcot-Marie-Tooth Disease Type 1B |
- Outgoing r'ship
SUBCLASS_OFto/from Charcot-Marie-Tooth Disease Type 1(ID:disease_node_18867) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)