Familial Behcet-Like Autoinflammatory Syndrome
Disease ID: disease_node_15593
Connections displayed (default: 10).
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| Dbxref | MIM:616744 |
|---|---|
| Subclassof | DOID_0050736, DOID_0051000 |
| Data Source | DOID |
| Synonyms | A20 haploinsufficiency |
| Doid Label | familial Behcet-like autoinflammatory syndrome |
| Doid Description | An autoinflammatory disease that is characterized by characterized by ulceration of mucosal surfaces, particularly in the oral and genital areas and that has_material_basis_in heterozygous mutation in the TNFAIP3 gene on chromosome 6q23. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_15593 |
| Doid Id | DOID_0080944 |
| Label | Familial Behcet-Like Autoinflammatory Syndrome |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autoinflammatory Disease(ID:disease_node_15587) (Disease)