Source:http://linkedlifedata.com/resource/lhgdn/association:46792
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
A patient represents a typical case of juvenile onset primary familial erythromelalgia, a rare disorder that has been shown in some patients to be caused by a mutation to the SCN9A gene.
|
| lhgdn:mesh_code |
D004916
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |