Source:http://linkedlifedata.com/resource/lhgdn/association:5630
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
CHD7 mutations can be present in Kallmann syndrome patients who have additional features that are part of the CHARGE syndrome phenotype
|
| lhgdn:mesh_code |
D017436
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |