Charcot-Marie-Tooth Disease Axonal Type 2P
Disease ID: disease_node_18851
Connections displayed (default: 10).
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| Dbxref | GARD:12435, ICD10CM:G60.0, MIM:614436, ORDO:300319 |
|---|---|
| Subclassof | DOID_0050736, DOID_0050737, DOID_0050539 |
| Data Source | DOID |
| Synonyms | CMT2P, Charcot-Marie-Tooth disease type 2P, Charcot-Marie-Tooth neuropathy type 2P |
| Doid Label | Charcot-Marie-Tooth disease axonal type 2P |
| Doid Description | A Charcot-Marie-Tooth disease type 2 that has_material_basis_in homozygous or heterozygous mutation in the LRSAM1 gene on chromosome 9q33. |
| Has Material Basis In | GENO_0000147, GENO_0000148 |
| Disease Node Id | disease_node_18851 |
| Doid Id | DOID_0110169 |
| Label | Charcot-Marie-Tooth Disease Axonal Type 2P |
- 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)