Source:http://linkedlifedata.com/resource/lhgdn/association:42436
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
The complex phenotype with Kallmann syndrome and bone anomalies observed in the patient could be the result of the interruption of the AKAP2 gene.
|
| lhgdn:mesh_code |
D017436
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |