Charcot-Marie-Tooth disease that has material basis in X-linked inheritance of a point mutation in the connexin-32 gene
| Property | Value |
|---|---|
| dbo:alias |
|
| dbo:description |
|
| dbp:causes | |
| dbp:complications |
|
| dbp:deaths |
|
| dbp:duration |
|
| dbp:frequency |
|
| dbp:name |
|
| dbp:onset |
|
| dbp:prevention |
|
| dbp:prognosis |
|
| dbp:specialty | |
| dbp:symptoms |
|
| dbp:synonyms |
|
| dbp:types |
|
| dbp:wikiPageUsesTemplate | |
| dct:subject | |
| rdf:type | |
| rdfs:label |
|
| prov:wasDerivedFrom | |
| foaf:isPrimaryTopicOf | |
| is foaf:primaryTopic of |