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Term:
AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS (DOID:9007910)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (0) Bonobo: (1) Dog: (1) Squirrel: (1)
Parent Terms Term With Siblings Child Terms
arthritis +     
Inflammation +     
Skin Abnormalities +     
Absence of Fingerprints  
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  
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 Syndrome Type 1  
Blepharophimosis Syndrome Type 2  
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 +   
chondrocalcinosis +   
cocoon syndrome  
Collagenosis, Familial Reactive Perforating 
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 +   
Deficiency of Interleukin-1 Receptor Antagonist  
Dermal Ridges, Nelson Syndrome 
Dermal Ridges, Patternless 
dermatitis +   
Dermoodontodysplasia 
Dowling-Degos disease +   
dyschromatosis universalis hereditaria +   
dyskeratosis congenita +   
Dyskeratosis, Hereditary Benign Intraepithelial 
ectodermal dysplasia +   
Ehlers-Danlos syndrome +   
encephalitis +   
encephalomyelitis +   
epidermolysis bullosa +   
Epithelial Squamous Dysplasia, Keratinizing Desquamative, of Urinary Tract 
Erosive Arthropathy 
erythrokeratodermia variabilis +   
Erythrokeratodermia with Ataxia  
Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa of Siemens-like  
Experimental Arthritis  
Familial Autoinflammatory Syndrome, Behcet-like  
Familial Dyskeratotic Comedones 
familial Mediterranean fever +   
Familial Popliteal Pterygium Syndrome 
fasciitis +  
Follicular Atrophoderma, Perioral Pigmented, with Milia and Epidermoid Cysts 
Foreign-Body Reaction +   
gastroenteritis +   
Gerodermia Osteodysplastica  
gout +   
Hailey-Hailey disease  
Hairy Palms and Soles 
Hepatic Porphyrias +   
Hereditary Autoinflammatory Diseases +   
hereditary mucosal leukokeratosis  
Histiocytic Dermatoarthritis 
Hyaluronan Metabolism, Defect in 
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 
Infantile Cataract, Skin Abnormalities, Glutamate Excess, and Impaired Intellectual Development  
Isolated Osteopoikilosis 
JMP syndrome  
Juvenile Spring Eruption of Ears 
Keratolytic Winter Erythema  
keratosis follicularis +   
Keratosis Follicularis Spinulosa Decalvans, X-Linked  
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma  
laryngitis +  
lethal restrictive dermopathy  
Leukoencephalopathy, Arthritis, Colitis, and Hypogammaglobulinemia 
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis 
LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2  
LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 3  
lipoid proteinosis  
meningitis +   
mevalonic aciduria  
Meyenburg-Altherr-Uehlinger Syndrome 
Michelin Tire Baby Syndrome +   
Microphthalmia, Syndromic 7  
monilethrix +   
Muir-Torre syndrome  
multicentric reticulohistiocytosis 
Multiple Noduli Cutanei with Urinary Tract Abnormalities 
multiple pterygium syndrome +   
myelitis +   
Negative Rheumatoid Factor Polyarthritis 
nephritis +   
neuritis +   
Neurogenic Inflammation  
Oculocerebrocutaneous Syndrome 
Oculotrichodysplasia 
orofaciodigital syndrome IX  
osteoarthritis +   
osteomyelitis +   
Otitis +   
otulipenia  
PALMOPLANTAR CARCINOMA, MULTIPLE SELF-HEALING  
palmoplantar keratosis +   
pancreatitis +   
Parana Hard Skin Syndrome 
Pedal Onychogryposis with Keratosis Plantaris and Coarse Hair 
peeling skin syndrome +   
periarthritis 
Perifolliculitis Capitis Abscedens Et Suffodiens, Familial 
Periodic Fever, Menstrual Cycle-Dependent  
periostitis +   
PFAPA Syndrome  
pharyngitis +   
Plasminogen Deficiency, Type I  
PLATELET ABNORMALITIES WITH EOSINOPHILIA AND IMMUNE-MEDIATED INFLAMMATORY DISEASE  
pneumonia +   
poikiloderma with neutropenia  
Poikiloderma, Hereditary Sclerosing +   
porokeratosis +   
Port-Wine Stain +   
primary cutaneous amyloidosis  
Primary Localized Cutaneous Amyloidosis, 2  
Primary Localized Cutaneous Amyloidosis, 3  
Progressive Osseous Heteroplasia  
Progressive Vitiligo with Mental Retardation and Urethral Duplication 
Prolidase Deficiency  
PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 2  
PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 3  
pseudoxanthoma elasticum +   
psoriatic arthritis  
Pterygium Colli, Isolated 
Rasmussen Subacute Encephalitis 
Reticulate Pigmentary Disorder, with Systemic Manifestations  
rheumatic disease +   
rheumatic fever +   
rheumatoid arthritis +   
rhinitis +   
Ridges-off-the-end Syndrome 
Rothmund-Thomson syndrome +   
Sacroiliac Arthritis 
Sacroiliitis  
Sclerema Neonatorum 
septic arthritis +   
Seroma 
Serositis  
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, INFANTILE-ONSET  
Storm Syndrome 
Suppuration +   
Supraglottitis +  
Systemic Hyalinosis  
Systemic Inflammatory Response Syndrome +   
thyroiditis +   
tracheitis 
transient arthritis +  
Trichothiodystrophy Syndromes +   
Urban Schosser Spohn Syndrome 
Vascular Hyalinosis 
vesiculitis +  
Vohwinkel Syndrome, Variant Form  
Winter Shortland Temple Syndrome  
X-linked ichthyosis +   
xeroderma pigmentosum +   

Synonyms
Exact Synonyms: AIADK
Primary IDs: OMIM:617388 ;   RDO:9001687

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