Charcot-Marie-Tooth Disease Type 4D
Disease ID: disease_node_18834
Connections displayed (default: 10).
Loading graph...
| Dbxref | ICD10CM:G60.0, MIM:601455, ORDO:99950 |
|---|---|
| Subclassof | DOID_0050737, DOID_0050541 |
| Data Source | DOID |
| Synonyms | CMT4D, Charcot-Marie-Tooth neuropathy type 4D, HMSN Lom type, HMSN-Lom, HMSN4D, HMSNL, autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4D, hereditary motor and sensory neuropathy LOM type |
| Doid Label | Charcot-Marie-Tooth disease type 4D |
| Doid Description | A Charcot-Marie-Tooth disease type 4 that has_material_basis_in homozygous mutation in the N-myc downstream-regulated gene-1 (NDRG1) on chromosome 8q24. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_18834 |
| Doid Id | DOID_0110186 |
| Label | Charcot-Marie-Tooth Disease Type 4D |
- 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)