Source:http://linkedlifedata.com/resource/lhgdn/association:10066
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
Mutations in GJB2, encoding the gap junction beta-2 protein Connexin 26, are associated with autosomal recessive nonsyndromic sensorineural hearing loss (NSHL), autosomal dominant NSHL, and several forms of syndromic sensorineural hearing loss
|
| lhgdn:mesh_code |
D006319
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |