Charcot-Marie-Tooth Disease Axonal Type 2T
Disease ID: disease_node_18860
Connections displayed (default: 10).
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| Dbxref | ICD10CM:G60.0, MIM:617017, ORDO:443950 |
|---|---|
| Subclassof | DOID_0050736, DOID_0050737, DOID_0050539 |
| Data Source | DOID |
| Synonyms | AR-CMT2T, CMT2T, Charcot-Marie-Tooth neuropathy type 2T, autosomal recessive axonal Charcot-Marie-Tooth disease type 2T |
| Doid Label | Charcot-Marie-Tooth disease axonal type 2T |
| Doid Description | A Charcot-Marie-Tooth disease type 2 that has_material_basis_in homozygous or compound heterozygous mutation in the MME gene on chromosome 3q25. |
| Has Material Basis In | GENO_0000147, GENO_0000148 |
| Disease Node Id | disease_node_18860 |
| Doid Id | DOID_0110160 |
| Label | Charcot-Marie-Tooth Disease Axonal Type 2T |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - 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 2(ID:disease_node_18839) (Disease)