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
This disease is an autosomal recessive disorder characterized by severe anemia and thrombocytopenia apparent from early infancy, hepatosplenomegaly, and recurrent fevers associated with a hyperinflammatory state. Laboratory studies show increased levels of proinflammatory cytokines and increased expression of interferon-stimulated genes (ISGs).
Banti's Syndrome
Behcet's disease
Chediak-Higashi syndrome +
Chronic recurrent multifocal osteomyelitis 2, with periostitis and pustulosis
Cryopyrin-Associated Periodic Syndromes +
Familial Autoinflammatory Syndrome, with or without Immunodeficiency
familial Mediterranean fever +
Fanconi-like syndrome
IMMUNE DYSREGULATION, AUTOIMMUNITY, AND AUTOINFLAMMATION
Immunodeficiency 111
immunodeficiency 115
immunodeficiency 133
immunodeficiency 94
immunodeficiency 97
immunodeficiency 98
mevalonic aciduria
Myelocerebellar Disorder
otulipenia
Pancytopenia and Occlusive Vascular Disease
Periodic Fever, Menstrual Cycle-Dependent
PFAPA syndrome
proteosome-associated autoinflammatory syndrome +
Sackey Sakati Aur Syndrome
STING-associated vasculopathy with onset in infancy