Source:http://linkedlifedata.com/resource/lhgdn/association:8591
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
A PEX6-defective peroxisomal biogenesis disorder with severe phenotype in an infant, versus mild phenotype resembling Usher syndrome in the affected parents
|
| lhgdn:mesh_code |
D052245
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |