Source:http://linkedlifedata.com/resource/lhgdn/association:5758
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
two mutations in the gene PCSK9 (encoding proprotein convertase subtilisin/kexin type 9) that cause autosomal dominant hypercholesterolemia
|
| lhgdn:mesh_code |
D006938
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |