Source:http://linkedlifedata.com/resource/lhgdn/association:59213
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
Sorting nexin 3 (SNX3) is disrupted in a patient with a translocation t (6; 13) (q21; q12) and microcephaly, microphthalmia, ectrodactyly, prognathism (MMEP) phenotype
|
| lhgdn:mesh_code |
D008831
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |