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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
Acute Anterior Uveitis +   
alveolar periostitis 
angioedema +   
angioma serpiginosum +  
antiphospholipid syndrome +   
aortitis  
Arteritis +   
autoimmune atherosclerosis 
autoimmune cardiomyopathy 
autoimmune myocarditis +   
autoimmune vasculitis 
Autoinflammation with Arthritis and Dyskeratosis  
Autoinflammation with Episodic Fever and Lymphadenopathy  
Autoinflammation with Infantile Enterocolitis  
Autoinflammation with Pulmonary and Cutaneous Vasculitis  
Autoinflammation, Antibody Deficiency, and Immune Dysregulation, PLCG2-Associated  
Autoinflammation, Immune Dysregulation, and Eosinophilia  
AUTOINFLAMMATORY DISEASE, MULTISYSTEM, WITH IMMUNE DYSREGULATION, X-LINKED  
AUTOINFLAMMATORY-PANCYTOPENIA SYNDROME  
autosomal dominant familial periodic fever  
bacillary angiomatosis 
Behcet's disease  
A vasculitis that is characterized by an autoimmune mediated inflammation of the blood vessels throughout the body leading to ulcerations on the mouth and sometimes the genitals, notorious for causing hypopyon uveitis. (DO)
bejel 
burning mouth syndrome +  
central nervous system vasculitis +   
Chediak-Higashi syndrome +   
Chronic Anterior Uveitis  
Cogan syndrome +   
cryoglobulinemic vasculitis  
Cryopyrin-Associated Periodic Syndromes +   
Cutaneous Small Vessel Lymphocytic Vasculitis 
Cutis Marmorata Telangiectatica Congenita 
Deficiency of Interleukin-1 Receptor Antagonist  
Edentulous Mouth +   
facial hemiatrophy 
facial nerve disease +   
Familial Autoinflammatory Syndrome, with or without Immunodeficiency  
familial mediterranean fever +   
focal epithelial hyperplasia 
Gardner-Diamond Syndrome 
granulomatous angiitis 
Granulomatous Vasculitis  
Hemifacial Spasm +   
herpangina +  
hypersensitivity vasculitis +   
IMMUNE DYSREGULATION, AUTOIMMUNITY, AND AUTOINFLAMMATION  
Immunodeficiency 113  
Immunodeficiency 115  
Immunodeficiency 94 with Autoinflammation and Dysmorphic Facies  
Immunodeficiency 97 with Autoinflammation  
Immunodeficiency 98 with Autoinflammation, X-Linked  
iridocyclitis +   
iritis 
Kawasaki disease  
Libman-Sacks endocarditis 
lip disease +   
Livedo Reticularis +   
livedoid vasculitis 
Ludwig's angina 
Malignant Atrophic Papulosis 
Megalencephaly - Cutis Marmorata Telangiectatica Congenita  
mevalonic aciduria  
Mouth Abnormalities +   
Mouth Neoplasms +   
mucositis +   
Nodular Lymphocytic Vasculitis 
noma +  
oral candidiasis  
oral cavity carcinoma in situ +   
Oral Fistula +  
oral hairy leukoplakia 
Oral Hemorrhage +  
oral leukoedema 
Oral Lichen Planus  
Oral Manifestations +   
oral mucosa leukoplakia +   
oral submucous fibrosis  
oral tuberculosis 
Oral Ulcer  
Orofacial Granulomatosis 
otulipenia  
Periodic Fever, Menstrual Cycle-Dependent  
periodontal disease +   
PFAPA Syndrome  
phlebitis +   
polyarteritis nodosa +   
proteosome-associated autoinflammatory syndrome +   
pyoderma gangrenosum +   
retinal vasculitis +   
rheumatic pulmonary valve disease 
salivary gland disease +   
Shwartzman phenomenon  
Sneddon syndrome  
STING-associated vasculopathy with onset in infancy  
stomatitis +   
Systemic Autoinflammatory Disease with Vasculitis  
Systemic Autoinflammatory Disease, X-Linked  
Systemic Vasculitis +   
Takayasu's arteritis  
temporal arteritis  
thromboangiitis obliterans  
tongue disease +   
tooth disease +   
Trichomonas tenax trichomoniasis 
urticaria +   
Vasculitis of the Skin  
YAO SYNDROME  

Synonyms
Exact Synonyms: Adamantiades Behcet Disease ;   Adamantiades-Behcet Diseases ;   BD ;   Behcet Disease ;   Behcet Syndrome ;   Behcet Triple Symptom Complex ;   Behcet's Syndrome ;   Behcets Syndrome ;   Behet's syndrome ;   Behçet Disease ;   Behçet Diseases ;   Old Silk Route Disease ;   triple symptom complex
Primary IDs: MESH:D001528
Alternate IDs: OMIM:109650
Xrefs: EFO:0003780 ;   GARD:848 ;   ICD10CM:M35.2 ;   ICD9CM:136.1 ;   NCI:C34416
Definition Sources: http://en.wikipedia.org/wiki/Beh%C3%A7et%27s_disease "DO" "DO", http://www.nlm.nih.gov/medlineplus/behcetssyndrome.html "DO" "DO"

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