Source:http://linkedlifedata.com/resource/lhgdn/association:33035
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
Most patients with AROA (autosomal recessive ocular albinism) represent phenotypically mild variants of oculocutaneous albinism, well over half of which is OCA1.
|
| lhgdn:mesh_code |
D016117
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |