Charcot-Marie-Tooth Disease X-Linked Recessive 4
Disease ID: disease_node_18823
Connections displayed (default: 10).
Loading graph...
| Dbxref | ICD10CM:G60.0, MIM:310490, ORDO:101078 |
|---|---|
| Subclassof | DOID_0080012, DOID_0050542 |
| Data Source | DOID |
| Synonyms | CMT4X, CMTX4, Charcot-Marie-Tooth disease with deafness and mental retardation, Cowchock syndrome, NADMR, NAMSD, X-linked Charcot-Marie-Tooth disease type 4, axonal motor sensory neuropathy with deafness and mental retardation |
| Doid Label | Charcot-Marie-Tooth disease X-linked recessive 4 |
| Doid Description | A Charcot-Marie-Tooth disease X-linked that has_material_basis_in mutation in the AIFM1 gene on chromosome Xq26. |
| Has Material Basis In | GENO_0000149 |
| Disease Node Id | disease_node_18823 |
| Doid Id | DOID_0110212 |
| Label | Charcot-Marie-Tooth Disease X-Linked Recessive 4 |
- Outgoing r'ship
SUBCLASS_OFto/from X-Linked Recessive Disease(ID:disease_node_13254) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Charcot-Marie-Tooth Disease Type X(ID:disease_node_18822) (Disease)