Source:http://linkedlifedata.com/resource/lhgdn/association:39993
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
Deficiency of and mutations and variations in the complement factor H (CFH) gene are associated with the development of membranoproliferative glomerulonephritis type II.
|
| lhgdn:mesh_code |
D015432
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |