Charcot-Marie-Tooth Disease Type 4F
Disease ID: disease_node_18831
Connections displayed (default: 10).
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| Dbxref | ICD10CM:G60.0, MIM:614895, ORDO:99952 |
|---|---|
| Subclassof | DOID_0050737, DOID_0050541 |
| Data Source | DOID |
| Synonyms | CMT4F |
| Doid Label | Charcot-Marie-Tooth disease type 4F |
| Doid Description | A Charcot-Marie-Tooth disease type 4 that has_material_basis_in homozygous or compound heterozygous mutation in the periaxin gene (PRX) on chromosome 19q13. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_18831 |
| Doid Id | DOID_0110193 |
| Label | Charcot-Marie-Tooth Disease Type 4F |
- 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)