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Term:
Keratolytic Winter Erythema (DOID:9003833)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (0)
Parent Terms Term With Siblings Child Terms
Erythema +     
keratosis +     
Absence of Fingerprints  
acquired hyperkeratosis 
acrokeratosis verruciformis  
actinic keratosis +   
Actinic Prurigo  
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  
Callosities +  
cholesteatoma +   
Collagenosis, Familial Reactive Perforating 
Congenital Erythroderma with Palmoplantar Keratoderma, Hypotrichosis, and Hyper-IgE  
Curly Hair-Acral Keratoderma-Caries Syndrome 
Cutaneous Bullous Amyloidosis 
cutaneous porphyria  
cutis laxa +   
Dowling-Degos disease +   
dyschromatosis universalis hereditaria +   
dyskeratosis congenita +   
ectodermal dysplasia +   
Ehlers-Danlos syndrome +   
epidermolysis bullosa +   
Epidermolysis Bullosa Simplex with Migratory Circinate Erythema  
Erythema Chronicum Migrans 
Erythema Induratum 
erythema infectiosum +   
erythema multiforme +   
Erythema Nodosum +   
erythrokeratodermia variabilis +   
Erythrokeratodermia with Ataxia  
Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa of Siemens-like  
Follicular Atrophoderma, Perioral Pigmented, with Milia and Epidermoid Cysts 
Gerodermia Osteodysplastica  
Hailey-Hailey disease  
Hepatic Porphyrias +   
Hereditary Autoinflammatory Diseases +   
hereditary mucosal leukokeratosis  
hereditary papulotranslucent acrokeratoderma 
Histiocytic Dermatoarthritis 
Hooft Disease 
Hyaluronan Metabolism, Defect in 
Hyperkeratosis Lenticularis Perstans 
ichthyosis +   
ichthyosis vulgaris +   
Isolated Osteopoikilosis 
Johnston Aarons Schelley 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  
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis 
lipoid proteinosis  
monilethrix +   
Muir-Torre syndrome  
Multiple Eruptive Milia 
Multiple Noduli Cutanei with Urinary Tract Abnormalities 
Oculotrichodysplasia 
orofaciodigital syndrome IX  
palmoplantar keratosis +   
Parakeratosis  
Parana Hard Skin Syndrome 
Pedal Onychogryposis with Keratosis Plantaris and Coarse Hair 
peeling skin syndrome +   
PEELING SKIN WITH LEUKONYCHIA, ACRAL PUNCTATE KERATOSES, CHEILITIS, AND KNUCKLE PADS  
Perifolliculitis Capitis Abscedens Et Suffodiens, Familial 
Plasminogen Deficiency, Type I  
Poikiloderma, Hereditary Sclerosing +   
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  
pseudoxanthoma elasticum +   
Reticulate Pigmentary Disorder, with Systemic Manifestations  
Rothmund-Thomson syndrome +   
Sclerotylosis 
seborrheic keratosis +   
Sjogren-Larsson syndrome +   
Skin Fragility-Woolly Hair Syndrome  
Stiff Skin Syndrome  
Storm Syndrome 
Sweet Syndrome  
Systemic Hyalinosis  
Trichostasis Spinulosa 
Trichothiodystrophy Syndromes +   
Urban Schosser Spohn Syndrome 
Vohwinkel Syndrome, Variant Form  
X-linked ichthyosis +   
xeroderma pigmentosum +   

Synonyms
Exact Synonyms: Erythrokeratolysis hiemalis ichthyosis ;   KWE ;   OUDTSHOORN SKIN DISEASE ;   Oudtshoorn skin
Primary IDs: MESH:C536155 ;   RDO:0001617
Alternate IDs: OMIM:148370

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