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Term:
Histiocytic Dermatoarthritis (DOID:9001944)
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Parent Terms Term With Siblings Child Terms
arthritis +     
Absence of Fingerprints  
achromatopsia 4  
Achromatopsia 5  
Acrootoocular Syndrome 
Actinic Prurigo  
Aicardi syndrome 
Alacrima +   
Albinism +   
aniridia +   
Annular Erythema 
arterial tortuosity syndrome  
ataxia with oculomotor apraxia type 3  
Ataxia-Microcephaly-Cataract Syndrome 
Ataxia-Oculomotor Apraxia 4  
atopic dermatitis +   
Atrophia Maculosa Varioliformis Cutis, Familial 
AUTOIMMUNE INTERSTITIAL LUNG, JOINT, AND KIDNEY DISEASE  
AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS  
autosomal recessive congenital ichthyosis +   
basal laminar drusen  
Basaloid Follicular Hamartoma Syndrome, Generalized, Autosomal Dominant 
bestrophinopathy  
Blau syndrome  
Bloch-Sulzberger syndrome +   
Bothnia retinal dystrophy  
bradyopsia  
bullous congenital ichthyosiform erythroderma  
Buschke-Ollendorff Syndrome  
cataract 17 multiple types  
cataract 22 multiple types  
cataract 35 
Cataract, Floriform 
Cataract, Pulverulent 
Cavitary Optic Disc Anomalies  
Cholestasis with Gallstone, Ataxia, and Visual Disturbance 
chondrocalcinosis +   
Choroideremia +   
Collagenosis, Familial Reactive Perforating 
cone-rod dystrophy +   
Congenital Alacrima +   
Congenital Erythroderma with Palmoplantar Keratoderma, Hypotrichosis, and Hyper-IgE  
Congenital Fibrosis of Extraocular Muscles, 2  
Congenital Fibrosis of Extraocular Muscles, 3A, with or without Extraocular Involvement  
Congenital Fibrosis of Extraocular Muscles, 3B  
Congenital Fibrosis of Extraocular Muscles, 3C 
Congenital Fibrosis of Extraocular Muscles, 5  
Congenital Mydriasis +   
Cornea Plana 1 
Cornea Plana 2  
corneal dystrophy +   
Cutaneous Bullous Amyloidosis 
cutaneous porphyria  
cutis laxa +   
Dowling-Degos disease +   
Duane retraction syndrome +   
dyschromatosis universalis hereditaria +   
dyskeratosis congenita +   
ectodermal dysplasia +   
Ehlers-Danlos syndrome +   
enhanced S-cone syndrome  
epidermolysis bullosa +   
erythrokeratodermia variabilis +   
Erythrokeratodermia with Ataxia  
Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa of Siemens-like  
Experimental Arthritis  
Fleck Retina, Familial Benign  
Follicular Atrophoderma, Perioral Pigmented, with Milia and Epidermoid Cysts 
Foveal Hypoplasia with Anterior Segment Anomalies  
Gerodermia Osteodysplastica  
Glaucoma 1, Open Angle, P  
gout +   
Graves Ophthalmopathy  
Grouped Pigmentation of the Macula 
gyrate atrophy +   
Hailey-Hailey disease  
Hepatic Porphyrias +   
Hereditary Autoinflammatory Diseases +   
hereditary mucosal leukokeratosis  
hereditary night blindness +   
Hereditary Optic Atrophies +   
high hyperopia  
Histiocytic Dermatoarthritis 
Hyaluronan Metabolism, Defect in 
ichthyosis vulgaris +   
Iris Pigment Epithelium Anomalies 
Isolated Foveal Hypoplasia 
Isolated Osteopoikilosis 
Joubert syndrome 8  
Juvenile Spring Eruption of Ears 
Keratolytic Winter Erythema  
keratosis follicularis +   
Keratosis Follicularis Spinulosa Decalvans, X-Linked  
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma  
Leber congenital amaurosis +   
Leukoencephalopathy, Arthritis, Colitis, and Hypogammaglobulinemia 
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis 
lipoid proteinosis  
Macular Dystrophy, X-Linked +   
megalocornea +   
Meyenburg-Altherr-Uehlinger Syndrome 
microcephaly and chorioretinopathy 1 +   
monilethrix +   
Muir-Torre syndrome  
multicentric reticulohistiocytosis 
Multiple Noduli Cutanei with Urinary Tract Abnormalities 
Negative Rheumatoid Factor Polyarthritis 
Oculotrichodysplasia 
Omphalocele, Diaphragmatic Hernia, and Radial Ray Defects 
Ophthalmomandibulomelic Dysplasia 
orofaciodigital syndrome IX  
osteoarthritis +   
palmoplantar keratosis +   
Parana Hard Skin Syndrome 
Pedal Onychogryposis with Keratosis Plantaris and Coarse Hair 
peeling skin syndrome +   
periarthritis 
Perifolliculitis Capitis Abscedens Et Suffodiens, Familial 
Peripapillary Atrophy, Beta Type 
Persistent Hyperplastic Primary Vitreous, Autosomal Recessive  
Pigmented Paravenous Chorioretinal Atrophy  
Plasminogen Deficiency, Type I  
Poikiloderma, Hereditary Sclerosing +   
PORETTI-BOLTSHAUSER SYNDROME  
porokeratosis +   
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  
pseudopapilledema 
pseudoxanthoma elasticum +   
psoriatic arthritis  
Radial Drusen, Autosomal Dominant 
renal hypomagnesemia 5 with ocular involvement  
Reticulate Pigmentary Disorder, with Systemic Manifestations  
Retinal Aplasia 
Retinal Dysplasia +   
Retinal Dystrophy, Early Onset Severe  
retinitis pigmentosa +   
Retinohepatoendocrinologic Syndrome 
Rhegmatogenous Retinal Detachment, Autosomal Dominant  
rheumatic fever +   
rheumatoid arthritis +   
Rothmund-Thomson syndrome +   
Sacroiliac Arthritis 
Sacroiliitis  
septic arthritis +   
Sjogren-Larsson syndrome +   
Skin Fragility-Woolly Hair Syndrome  
Spondylarthritis +   
Spondyloocular Syndrome, Autosomal Recessive  
Stickler Syndrome, Type I, Nonsyndromic Ocular  
Stiff Skin Syndrome  
Storm Syndrome 
Systemic Hyalinosis  
transient arthritis +  
Trichothiodystrophy Syndromes +   
Vascular Hyalinosis 
vitelliform macular dystrophy +   
Vitreoretinochoroidopathy  
Vitreoretinopathy with Phalangeal Epiphyseal Dysplasia  
Vohwinkel Syndrome, Variant Form  
Walker-Warburg syndrome +   
Weill-Marchesani syndrome +   
X-linked ichthyosis +   
xeroderma pigmentosum +   

Synonyms
Primary IDs: MESH:C564183 ;   RDO:0013226

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