Source:http://linkedlifedata.com/resource/lhgdn/association:36533
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
Primary microcephaly is an autosomal-recessive congenital disorder characterized by smaller brain size and mental retardation, in which homozygote mutations in STIL proteins are found.
|
| lhgdn:mesh_code |
D008831
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |