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.