| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_11983) |
| External Link | http://www.omim.org/entry/176270 |
| Similar Terms | |
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2 genes associated with the prader-willi syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
