Source:http://linkedlifedata.com/resource/lhgdn/association:62600
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
A mutation in this gene causes X-linked cone dystrophy/type of hereditary retinal degeneration is distinct from retinitis pigmentosa.
|
| lhgdn:mesh_code |
D012174
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |