Source:http://linkedlifedata.com/resource/lhgdn/association:59208
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
The phenotype of renal agenesis/dysgenesis strongly indicates the existence of KAL1 gene defects in the genotype of patients with sporadic Kallmann syndrome.
|
| lhgdn:mesh_code |
D017436
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |