Charcot-Marie-Tooth Disease Type 1
Disease ID: disease_node_18867
Connections displayed (default: 10).
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| Dbxref | GARD:12433 |
|---|---|
| Subclassof | DOID_10595 |
| Data Source | DOID |
| Synonyms | hereditary motor and sensory neuropathy type 1 |
| Doid Label | Charcot-Marie-Tooth disease type 1 |
| Doid Description | A Charcot-Marie-Tooth disease characterized by demyelination of the peripheral nerve axons. OMIM mapping confirmed by DO. [SN]. |
| Disease Node Id | disease_node_18867 |
| Doid Id | DOID_0050538 |
| Label | Charcot-Marie-Tooth Disease Type 1 |
- Incoming r'ship
SUBCLASS_OFto/from Charcot-Marie-Tooth Disease Type 1G(ID:disease_node_18868) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Charcot-Marie-Tooth Disease Type 1A(ID:disease_node_18872) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Charcot-Marie-Tooth Disease Type 1B(ID:disease_node_18870) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Charcot-Marie-Tooth Disease Type 1F(ID:disease_node_18871) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Charcot-Marie-Tooth Disease Type 1E(ID:disease_node_18869) (Disease)