Source:http://linkedlifedata.com/resource/lhgdn/association:26207
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
SMPD1 mutation (r608del) is prevalent among Niemann-Pick disease type b patients from the North-African Maghreb region.
|
| lhgdn:mesh_code |
D009542
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |