| Dataset | DISEASES Curated Gene-Disease Association Evidence Scores |
| Category | disease or phenotype associations |
| Type | disease |
| Description | An autosomal dominant disease characterized by familial granulomatous arthritis, uveitis and skin granulomas caused_by NOD2/CARD15 mutations. (Human Disease Ontology, DOID_0050678) |
| Similar Terms | |
| Downloads & Tools |
1 genes involed in the disease blau syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
| Symbol | Name |
|---|---|
| NOD2 | nucleotide-binding oligomerization domain containing 2 |
