| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | An autosomal dominant disease characterized by familial granulomatous arthritis, uveitis and skin granulomas caused_by NOD2/CARD15 mutations. (Human Disease Ontology, DOID_0050678) |
| External Link | http://www.omim.org/entry/186580 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the blau syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| NOD2 | nucleotide-binding oligomerization domain containing 2 |
