Source:http://linkedlifedata.com/resource/lhgdn/association:10042
Predicate | Object |
---|---|
lhgdn:found_in | |
lhgdn:geneRifSource |
findings identify a cohort of 33 probands with pathogenic GJB2 mutations who have additional structural and/or developmental abnormalities beyond the bilateral sensorineural hearing loss, or who already had an established etiology for their hearing loss
|
lhgdn:mesh_code |
D006319
|
lhgdn:associationIdType | |
lhgdn:umls_code |