Source:http://linkedlifedata.com/resource/lhgdn/association:14264
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
Range of the clinical phenotype caused by GCK mutations varies from complete insulin deficiency to extreme hyperinsulinemia.
|
| lhgdn:mesh_code |
D006946
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |