Source:http://linkedlifedata.com/resource/lhgdn/association:12377
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
homozygous mutations in DEHAL1 appear to cause human iodotyrosine deiodinase deficiency, leading to hereditary hypothyroidism and goiter
|
| lhgdn:mesh_code |
D006042
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |