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Ontology Browser

Autoinflammation with Arthritis and Dyskeratosis (DOID:9007910)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (0) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
arthritis +     
Inflammation +     
Skin Abnormalities +     
acrodermatitis +   
Actinic Prurigo  
Acute-Phase Reaction  
Albinism +   
Anetoderma +   
Annular Erythema 
arterial tortuosity syndrome  
atopic dermatitis +   
Atrophia Maculosa Varioliformis Cutis, Familial 
Autoimmune Interstitial Lung, Joint, and Kidney Disease  
Autoinflammation with Arthritis and Dyskeratosis  
A disease characterized by recurrent fever, widespread skin dyskeratosis, arthritis, elevated biologic markers of inflammation, and mild autoimmunity with a high transitional B-cell level. (OMIM)
Autoinflammation with Infantile Enterocolitis  
Autoinflammation, Antibody Deficiency, and Immune Dysregulation, PLCG2-Associated  
Autoinflammation, Immunde Dysregulation, and Eosinophilia  
autosomal dominant familial periodic fever  
autosomal recessive congenital ichthyosis +   
Barber-Say syndrome  
Basaloid Follicular Hamartoma Syndrome, Generalized, Autosomal Dominant 
Beare-Stevenson cutis gyrata syndrome  
Behcet's disease  
Blau syndrome  
Blepharophimosis with Ptosis, Syndactyly, and Short Stature 
blepharophimosis, ptosis, and epicanthus inversus syndrome +   
Bloch-Sulzberger syndrome +   
Book Syndrome 
bronchitis +   
bullous congenital ichthyosiform erythroderma  
Buschke-Ollendorff syndrome  
C1q Deficiency  
Carney complex +   
cherubism +   
chondrocalcinosis +   
Congenital Erythroderma with Palmoplantar Keratoderma, Hypotrichosis, and Hyper-IgE  
Cryopyrin-Associated Periodic Syndromes +   
Cutaneous Bullous Amyloidosis 
Cutaneous Hemangiomatosis with Associated Features 
cutaneous porphyria  
cutis laxa +   
Defect in Hyaluronan Metabolism 
Deficiency of Interleukin-1 Receptor Antagonist  
Dermal Ridges, Nelson Syndrome 
dermatitis +   
Dowling-Degos disease +   
dyschromatosis universalis hereditaria +   
dyskeratosis congenita +   
ectodermal dysplasia +   
Ehlers-Danlos syndrome +   
encephalitis +   
encephalomyelitis +   
epidermolysis bullosa +   
epidermolytic hyperkeratosis +   
Epithelial Squamous Dysplasia, Keratinizing Desquamative, of Urinary Tract 
Erosive Arthropathy 
erythrokeratodermia variabilis +   
Erythrokeratodermia with Ataxia 
Experimental Arthritis  
Familial Autoinflammatory Syndrome, with or without Immunodeficiency  
familial Behcet-like autoinflammatory syndrome  
Familial Dyskeratotic Comedones 
familial Mediterranean fever +   
Familial Popliteal Pterygium Syndrome 
Familial Reactive Perforating Collagenosis 
fasciitis +   
fetal encasement syndrome  
Foreign-Body Reaction +   
gastroenteritis +   
geroderma osteodysplasticum  
gout +   
Hailey-Hailey disease  
Hairy Palms and Soles 
Hepatic Porphyrias +   
Hereditary Autoinflammatory Diseases +   
Hereditary Benign Intraepithelial Dyskeratosis 
hereditary mucosal leukokeratosis  
Hereditary Sclerosing Poikiloderma +   
Histiocytic Dermatoarthritis 
hyaline fibromatosis syndrome  
Hyperkeratotic Cutaneous Capillary-Venous Malformations Associated with Cerebral Capillary Malformations  
Hypohidrosis with Abnormal Palmar Dermal Ridges 
ichthyosis +   
ichthyosis vulgaris +   
Ichthyosis-Mental Retardation Syndrome with Large Keratohyalin Granules in the Skin 
immunodeficiency 71  
Immunodeficiency 82  
Infantile Cataract, Skin Abnormalities, Glutamate Excess, and Impaired Intellectual Development  
Isolated Osteopoikilosis 
Isolated Pterygium Colli 
Juvenile Spring Eruption of Ears 
Keratolytic Winter Erythema  
keratosis follicularis +   
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma  
laryngitis +  
lethal restrictive dermopathy  
Leukoencephalopathy, Arthritis, Colitis, and Hypogammaglobulinemia 
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis 
lipoid proteinosis  
meningitis +   
mevalonic aciduria  
Meyenburg-Altherr-Uehlinger Syndrome 
MLS syndrome +   
monilethrix +   
Muir-Torre syndrome  
multicentric reticulohistiocytosis 
multiple benign circumferential skin creases on limbs +   
Multiple Noduli Cutanei with Urinary Tract Abnormalities 
multiple pterygium syndrome +   
Multiple Self-healing Palmoplantar Carcinoma  
myelitis +   
Negative Rheumatoid Factor Polyarthritis 
nephritis +   
neuritis +   
Neurogenic Inflammation  
Oculocerebrocutaneous Syndrome 
orofaciodigital syndrome IX  
osteoarthritis +   
osteomyelitis +   
Otitis +   
palmoplantar keratosis +   
pancreatitis +   
Parana Hard Skin Syndrome 
Patternless Dermal Ridges 
Pedal Onychogryposis with Keratosis Plantaris and Coarse Hair 
peeling skin syndrome +   
Perifolliculitis Capitis Abscedens Et Suffodiens, Familial 
Periodic Fever, Menstrual Cycle-Dependent  
Perioral Pigmented Follicular Atrophoderma with Milia and Epidermoid Cysts 
periostitis +   
PFAPA Syndrome  
pharyngitis +   
plasminogen deficiency type I  
pneumonia +   
poikiloderma with neutropenia  
porokeratosis +   
Port-Wine Stain +   
primary cutaneous amyloidosis +   
progressive osseous heteroplasia  
Progressive Vitiligo with Mental Retardation and Urethral Duplication 
prolidase deficiency  
Proteasome-Associated Autoinflammatory Syndromes +   
pseudoxanthoma elasticum +   
psoriatic arthritis  
Rasmussen Subacute Encephalitis 
rheumatic disease +   
rheumatic fever +   
rheumatoid arthritis +   
rhinitis +   
Ridges-off-the-end Syndrome 
Rothmund-Thomson syndrome +   
Sacroiliac Arthritis  
Sclerema Neonatorum 
septic arthritis +   
sinusitis +   
Sjogren-Larsson syndrome +   
Skin Fragility-Woolly Hair Syndrome  
Skin/Hair/Eye Pigmentation, Variation In, 1  
Skin/Hair/Eye Pigmentation, Variation In, 10  
Skin/Hair/Eye Pigmentation, Variation In, 11  
Skin/Hair/Eye Pigmentation, Variation In, 4  
Skin/Hair/Eye Pigmentation, Variation In, 5  
Skin/Hair/Eye Pigmentation, Variation In, 6  
Skin/Hair/Eye Pigmentation, Variation In, 7  
Skin/Hair/Eye Pigmentation, Variation In, 8  
Skin/Hair/Eye Pigmentation, Variation In, 9  
Spondylarthritis +   
spondylitis +   
stiff skin syndrome  
STING-associated vasculopathy with onset in infancy  
Storm Syndrome 
Suppuration +   
Supraglottitis +  
Systemic Inflammatory Response Syndrome +   
systemic lupus erythematosus +   
thyroiditis +   
transient arthritis +  
trichothiodystrophy +   
Urban Schosser Spohn Syndrome  
Vascular Hyalinosis 
vesiculitis +  
Vohwinkel Syndrome, Variant Form  
Winter Shortland Temple Syndrome  
X-linked ichthyosis +   
X-linked reticulate pigmentary disorder  
xeroderma pigmentosum +   

Exact Synonyms: AIADK
Primary IDs: OMIM:617388

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