Charcot-Marie-Tooth Disease Type 2A2A
Disease ID: disease_node_18862
Connections displayed (default: 10).
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| Dbxref | ICD10CM:G60.0, MIM:609260, ORDO:99947 |
|---|---|
| Subclassof | DOID_0050736, DOID_0050539 |
| Data Source | DOID |
| Synonyms | CMT2A2A, Charcot-Marie-Tooth neuronal type 2A2, Charcot-Marie-Tooth neuropathy type 2A2, HMSN IIA2, HMSN2A2, autosomal dominant axonal Charcot-Marie-Tooth disease type 2A2, hereditary motor and sensory neuropathy IIA2 |
| Doid Label | Charcot-Marie-Tooth disease type 2A2A |
| Doid Description | A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the MFN2 gene on chromosome 1p36.22. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_18862 |
| Doid Id | DOID_0110155 |
| Label | Charcot-Marie-Tooth Disease Type 2A2A |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Charcot-Marie-Tooth Disease Type 2(ID:disease_node_18839) (Disease)