Source:http://linkedlifedata.com/resource/lhgdn/association:47791
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
EYA1 mutations were found in 31% of families fitting established clinical criteria for branchio-oto-renal syndrome (BOR) and 7% of families with questionable BOR phenotype
|
| lhgdn:mesh_code |
D019280
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |