Source:http://linkedlifedata.com/resource/lhgdn/association:5625
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
CHD7 represents the first identified chromatin-remodeling protein with a role in human puberty and the second gene to cause both normosmic idiopathic hypogonadotropic hypogonadism and Kallmann syndrome in humans
|
| lhgdn:mesh_code |
D017436
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |