Source:http://linkedlifedata.com/resource/lhgdn/association:56259
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome.
|
| lhgdn:mesh_code |
D017436
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |