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Ontology Browser

Term:
Systemic Autoinflammatory Disease with Vasculitis (DOID:9000447)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1) Naked Mole-rat: (1) Green Monkey: (1)
Parent Terms Term With Siblings Child Terms
aortitis 
Arteritis +   
Autoinflammation with Arthritis and Dyskeratosis  
AUTOINFLAMMATION WITH ARTHRITIS AND VASCULITIS  
AUTOINFLAMMATION WITH EPISODIC FEVER AND IMMUNE DYSREGULATION  
Autoinflammation with Episodic Fever and Lymphadenopathy  
Autoinflammation with Infantile Enterocolitis  
Autoinflammation with Pulmonary and Cutaneous Vasculitis  
autoinflammation, antibody deficiency, and immune dysregulation syndrome  
Autoinflammation, Immune Dysregulation, and Eosinophilia  
AUTOINFLAMMATORY DISEASE, MULTISYSTEM, WITH IMMUNE DYSREGULATION, X-LINKED  
AUTOINFLAMMATORY-PANCYTOPENIA SYNDROME  
autosomal dominant familial periodic fever  
Behcet's disease  
central nervous system vasculitis +   
Chediak-Higashi syndrome +   
Chronic recurrent multifocal osteomyelitis 2, with periostitis and pustulosis  
Cogan syndrome +   
cryoglobulinemic vasculitis  
Cryopyrin-Associated Periodic Syndromes +   
Cutaneous Small Vessel Lymphocytic Vasculitis 
Familial Autoinflammatory Syndrome, with or without Immunodeficiency  
familial Mediterranean fever +   
granulomatous angiitis 
Granulomatous Vasculitis  
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  
Kawasaki disease  
livedoid vasculitis 
Malignant Atrophic Papulosis 
mevalonic aciduria  
Nodular Lymphocytic Vasculitis 
otulipenia  
Periodic Fever, Menstrual Cycle-Dependent  
PFAPA syndrome  
phlebitis +   
proteosome-associated autoinflammatory syndrome +   
retinal vasculitis +   
Shwartzman phenomenon  
STING-associated vasculopathy with onset in infancy  
Systemic Autoinflammatory Disease with Vasculitis  
An autosomal dominant disorder that manifests soon after birth with features such as purpuric skin rash, fever, hepatosplenomegaly, and elevated C-reactive protein (CRP). Caused by heterozygous mutation in the LYN gene on chromosome 8q13.
Systemic Autoinflammatory Disease, X-Linked  
Systemic Vasculitis +   
thromboangiitis obliterans  
Vasculitis of the Skin  
YAO SYNDROME  

Synonyms
Exact Synonyms: LAVLI syndrome ;   LYN-RELATED CONDITION ;   SAIDV
Primary IDs: MIM:620376
Definition Sources: MIM:620376

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