Bechet disease (BD) is a chronic, relapsing, multisystemic vasculitis characterized by mucocutaneous lesions, as well as articular, vascular, ocular and central nervous system manifestations. [ Orphanet:117 ]
Term information
- EFO:0003780 (MONDO:equivalentTo)
- DOID:13241 (MONDO:equivalentTo)
- UMLS:C0004943 (Orphanet:117)
- MedDRA:10004213 (Orphanet:117)
- COHD:436642 (MONDO:equivalentTo)
- ICD10:M35.2 (Orphanet:117)
- GARD:0000848 (Orphanet-shared)
- MESH:D001528 (Orphanet:117)
- SCTID:310701003 (MONDO:equivalentTo)
- Orphanet:117 (OMIM:109650)
- NCIT:C34416 (MONDO:equivalentTo)
- OMIM:109650 (Orphanet:117)
- ICD9:136.1 (i2s)
ordo_disease
Bechet disease (BD) is a chronic, relapsing, multisystemic vasculitis characterized by mucocutaneous lesions, as well as articular, vascular, ocular and central nervous system manifestations.
http://linkedlifedata.com/resource/umls/id/C0004943
http://purl.obolibrary.org/obo/DOID_13241
http://purl.obolibrary.org/obo/NCIT_C34416
http://www.orpha.net/ORDO/Orphanet_117
http://identifiers.org/mesh/D001528
http://identifiers.org/snomedct/310701003
http://identifiers.org/meddra/10004213
http://identifiers.org/omim/109650
Behçet's syndrome
Behcet's syndrome
Morbus Behçet's syndrome
Behçet disease
silk road disease
Behçet-Adamantiades syndrome
Bechet syndrome
triple symptom complex
Behçet syndrome
Behet's syndrome
Behcet syndrome
Adamantiades-Behcet disease
Behcet disease
Term relations
- inflammatory and autoimmune disease with epilepsy
- central nervous system vasculitis
- secondary glomerular disease
- systemic diseases with anterior uveitis
- systemic diseases with panuveitis
- predominantly large-vessel vasculitis
- systemic diseases with posterior uveitis
- autoinflammatory syndrome with skin involvement
- unclassified autoinflammatory syndrome
- skin vascular disease
- disease has location some blood vessel
- disease has feature some Uveitis