Source:http://linkedlifedata.com/resource/lhgdn/association:51362
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
" Mutations within HESX1 have been described in association with both dominant and recessive forms of septo-optic dysplasia, combined pituitary hormone deficiency and isolated growth hormone deficiency " p.207
|
| lhgdn:mesh_code |
D025962
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |