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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Actinic Prurigo  
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 +   
bullous congenital ichthyosiform erythroderma  
Buschke-Ollendorff syndrome  
Congenital Erythroderma with Palmoplantar Keratoderma, Hypotrichosis, and Hyper-IgE  
Cutaneous Bullous Amyloidosis 
cutaneous porphyria  
cutis laxa +   
Defect in Hyaluronan Metabolism 
Dowling-Degos disease +   
dyschromatosis universalis hereditaria +   
dyskeratosis congenita +   
ectodermal dysplasia +   
Ehlers-Danlos syndrome +   
epidermolysis bullosa +   
epidermolytic hyperkeratosis +   
erythrokeratodermia variabilis +   
Familial Behcet-Like Autoinflammatory Syndrome +   
familial cold autoinflammatory syndrome +   
Familial Reactive Perforating Collagenosis 
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 Sclerosing Poikiloderma +   
Histiocytic Dermatoarthritis 
hyaline fibromatosis syndrome  
ichthyosis vulgaris +   
Isolated Osteopoikilosis 
Juvenile Spring Eruption of Ears 
Keratolytic Winter Erythema  
keratosis follicularis +   
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma  
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis 
lipoid proteinosis  
monilethrix +   
Muir-Torre syndrome  
Multiple Noduli Cutanei with Urinary Tract Abnormalities 
Oculotrichodysplasia 
orofaciodigital syndrome IX  
palmoplantar keratosis +   
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 
plasminogen deficiency type I  
poikiloderma with neutropenia  
porokeratosis +   
primary cutaneous amyloidosis +   
progressive osseous heteroplasia  
Progressive Vitiligo with Mental Retardation and Urethral Duplication 
prolidase deficiency  
proteosome-associated autoinflammatory syndrome +   
pseudoxanthoma elasticum +   
Rothmund-Thomson syndrome +   
Sjogren-Larsson syndrome +   
spinocerebellar ataxia type 34  
stiff skin syndrome  
Storm Syndrome 
TNF receptor-associated periodic syndrome  
trichothiodystrophy +   
Vohwinkel Syndrome, Variant Form  
white sponge nevus +   
X-linked ichthyosis +   
X-linked reticulate pigmentary disorder  
xeroderma pigmentosum +   
 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  
 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 +   
 IMMUNE DYSREGULATION, AUTOIMMUNITY, AND AUTOINFLAMMATION  
 immunodeficiency 115  
 immunodeficiency 133  
 immunodeficiency 94  
 immunodeficiency 97  
 immunodeficiency 98  
 mevalonic aciduria  
 otulipenia  
 Periodic Fever, Menstrual Cycle-Dependent  
 PFAPA syndrome  
 proteosome-associated autoinflammatory syndrome +   
 STING-associated vasculopathy with onset in infancy  
 Systemic Autoinflammatory Disease with Vasculitis  
 Systemic Autoinflammatory Disease, X-Linked  
 TNF receptor-associated periodic syndrome  
 YAO SYNDROME  

Synonyms
Exact Synonyms: Reimann periodic disease ;   Siegal Cattan Mamou disease ;   hereditary autoinflammation disease ;   hereditary autoinflammation diseases ;   hereditary autoinflammatory disease ;   hereditary periodic fever syndromes ;   hereditary recurrent fever ;   hereditary recurrent fevers
Primary IDs: MESH:D056660
Definition Sources: MESH:D056660

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