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Term:
Hereditary Autoinflammatory Diseases (DOID:9006364)
Annotations: Rat: (108) Mouse: (110) Human: (113) Chinchilla: (94) Bonobo: (107) Dog: (111) Squirrel: (98) Pig: (102)
Parent Terms Term With Siblings Child Terms
Inflammation +     
Actinic Prurigo  
Acute-Phase Reaction  
adermatoglyphia  
Albinism +   
Annular Erythema 
arterial tortuosity syndrome  
atopic dermatitis +   
Atrophia Maculosa Varioliformis Cutis, Familial 
Autoinflammation with Arthritis and Dyskeratosis  
autosomal recessive congenital ichthyosis +   
Basaloid Follicular Hamartoma Syndrome, Generalized, Autosomal Dominant 
Bloch-Sulzberger syndrome +   
bronchitis +   
bullous congenital ichthyosiform erythroderma  
Buschke-Ollendorff syndrome  
cherubism +   
Collagenosis, Familial Reactive Perforating 
Congenital Erythroderma with Palmoplantar Keratoderma, Hypotrichosis, and Hyper-IgE  
Cutaneous Bullous Amyloidosis 
cutaneous porphyria  
cutis laxa +   
Defect in Hyaluronan Metabolism 
dermatitis +   
Dowling-Degos disease +   
dyschromatosis universalis hereditaria +   
dyskeratosis congenita +   
ectodermal dysplasia +   
Ehlers-Danlos syndrome +   
encephalitis +   
encephalomyelitis +   
epidermolysis bullosa +   
epidermolytic hyperkeratosis +   
erythrokeratodermia variabilis +   
Erythrokeratodermia with Ataxia 
Familial Autoinflammatory Syndrome, Behcet-like  
fasciitis +   
Foreign-Body Reaction +   
gastroenteritis +   
geroderma osteodysplasticum  
Hailey-Hailey disease  
Hepatic Porphyrias +   
Hereditary Autoinflammatory Diseases +   
Hereditary inflammation conditions, characterized by recurrent episodes of systemic inflammation. Common symptoms include recurrent fever, rash, arthritis, fatigue, and secondary AMYLOIDOSIS. Hereditary autoinflammatory diseases are associated with mutations in genes involved in regulation of normal inflammatory process and are not caused by AUTOANTIBODIES, or antigen specific T-LYMPHOCYTES.
hereditary mucosal leukokeratosis  
Hereditary Sclerosing Poikiloderma +   
Histiocytic Dermatoarthritis 
hyaline fibromatosis syndrome  
ichthyosis vulgaris +   
immunodeficiency 71  
Isolated Osteopoikilosis 
Juvenile Spring Eruption of Ears 
Keratolytic Winter Erythema  
keratosis follicularis +   
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma  
laryngitis +  
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis 
lipoid proteinosis  
meningitis +   
monilethrix +   
MUCOCUTANEOUS ULCERATION, CHRONIC  
Muir-Torre syndrome  
Multiple Noduli Cutanei with Urinary Tract Abnormalities 
myelitis +   
nephritis +   
neuritis +   
Neurogenic Inflammation  
Oculotrichodysplasia 
orofaciodigital syndrome IX  
osteomyelitis +   
Otitis +   
otulipenia  
palmoplantar keratosis +   
pancreatitis +   
Parana Hard Skin Syndrome 
Pedal Onychogryposis with Keratosis Plantaris and Coarse Hair 
peeling skin syndrome +   
Perifolliculitis Capitis Abscedens Et Suffodiens, Familial 
Perioral Pigmented Follicular Atrophoderma with Milia and Epidermoid Cysts 
periostitis +   
pharyngitis +   
plasminogen deficiency type I  
pneumonia +   
poikiloderma with neutropenia  
porokeratosis +   
primary cutaneous amyloidosis +   
progressive osseous heteroplasia  
Progressive Vitiligo with Mental Retardation and Urethral Duplication 
prolidase deficiency  
pseudoxanthoma elasticum +   
Rasmussen Subacute Encephalitis 
rheumatic disease +   
rhinitis +   
Rothmund-Thomson syndrome +   
Seroma 
Serositis  
sinusitis +   
Sjogren-Larsson syndrome +   
Skin Fragility-Woolly Hair Syndrome  
spondylitis +   
stiff skin syndrome  
Storm Syndrome 
Suppuration +   
Supraglottitis +  
Systemic Inflammatory Response Syndrome +   
systemic lupus erythematosus +   
thyroiditis +   
tracheitis 
trichothiodystrophy +   
vesiculitis +  
Vohwinkel Syndrome, Variant Form  
X-linked ichthyosis +   
X-linked reticulate pigmentary disorder  
xeroderma pigmentosum +   

Synonyms
Exact Synonyms: Hereditary Autoinflammatory Disease ;   Hereditary Recurrent Fever ;   Reimann periodic disease ;   Siegal Cattan Mamou disease ;   hereditary autoinflammation disease ;   hereditary autoinflammation diseases ;   hereditary periodic fever syndromes ;   hereditary recurrent fevers
Primary IDs: MESH:D056660
Xrefs: OMIM:PS256040
Definition Sources: MESH:D056660

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.