| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | No OMIM mapping, confirmed by DO. [SN]. (Human Disease Ontology, DOID_0050656) |
| External Link | http://www.omim.org/entry/251290 |
| Similar Terms | |
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1 genes associated with the band-like calcification with simplified gyration and polymicrogyria phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| OCLN | occludin |