Source:http://linkedlifedata.com/resource/lhgdn/association:63012
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
Loss-of-function mutations in PROK2 and PROKR2 underlie both Kallmann syndrome (KS) and normosmic idiopathic hypogonadotropic hypogonadism (IHH).
|
| lhgdn:mesh_code |
D017436
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |