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Term:
Parent Terms Term With Siblings Child Terms
skin disease +     
Achenbach syndrome 
Acneiform Eruptions +   
Actinic Prurigo  
ainhum +  
Albinism +   
allergic cutaneous vasculitis +   
Alpha-2-Deficient Collagen Disease 
ancylostomiasis +  
Anetoderma +   
angioedema +   
Annular Erythema 
arterial tortuosity syndrome  
atopic dermatitis +   
Atrophia Maculosa Varioliformis Cutis, Familial 
Au-Kline Syndrome  
AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS  
Basaloid Follicular Hamartoma Syndrome, Generalized, Autosomal Dominant 
Bloch-Sulzberger syndrome +   
bone disease +   
Bone Fragility with Contractures, Arterial Rupture, and Deafness  
Borrone Di Rocco Crovato Syndrome  
Boudhina Yedes Khiari syndrome 
breast disease +   
Buschke-Ollendorff Syndrome  
C Syndrome  
cartilage disease +   
cellulitis +   
cercarial dermatitis 
chancroid +  
chronic interstitial cystitis 
chronic ulcer of skin +   
coenurosis 
collagen disease +   
Collagenosis, Familial Reactive Perforating 
Congenital Erythroderma with Palmoplantar Keratoderma, Hypotrichosis, and Hyper-IgE  
Congenital Fascial Dystrophy 
congenital ichthyosiform erythroderma +   
Connective Tissue Neoplasms +   
contagious pustular dermatitis 
Cutaneous Bullous Amyloidosis 
Cutaneous Fistula 
cutaneous lupus erythematosus +   
cutaneous mycosis +   
cutaneous porphyria  
cutis laxa +   
A group of connective tissue diseases in which skin hangs in loose pendulous folds. It is believed to be associated with decreased elastic tissue formation as well as an abnormality in elastin formation. Cutis laxa is usually a genetic disease, but acquired cases have been reported. (From Dorland, 27th ed)
dental pulp disease +   
Dermal Fibrosis  
dermatitis +   
Dermatoleukodystrophy 
dermatomyositis +   
dipetalonemiasis 
Dowling-Degos disease +   
Duplication of Eyebrows with Stretchable Skin and Syndactyly 
Dupuytren Contracture +  
dyschromatosis universalis hereditaria +   
dyskeratosis congenita +   
Ectodermal Dysplasia +   
Ectodermal Dysplasia-Skin Fragility Syndrome  
Eczematous Skin Diseases +   
Ehlers-Danlos syndrome +   
Elastosis Perforans Serpiginosa 
Elliott Ludman Teebi Syndrome 
endometriosis in scar of skin 
enthesopathy +  
epidermal nevus +   
epidermolysis bullosa +   
epidermolytic hyperkeratosis +   
Erythema +   
erythematosquamous dermatosis 
erythrokeratodermia variabilis +   
Erythrokeratodermia with Ataxia  
exanthem +   
Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa of Siemens-like  
FACES Syndrome 
facial dermatosis +   
Facial Ectodermal Dysplasia  
fasciitis +  
fibrodysplasia ossificans progressiva  
filariasis +   
Fingerprints, Absence of  
Flynn Aird Syndrome 
Focal Facial Dermal Dysplasia 4  
Follicular Atrophoderma, Perioral Pigmented, with Milia and Epidermoid Cysts 
Foot Diseases +   
funisitis 
Genetic Skin Diseases +   
Gerodermia Osteodysplastica  
Hailey-Hailey disease  
hair disease +   
hand dermatosis +  
Hepatic Porphyrias +   
Hereditary Autoinflammatory Diseases +   
hereditary mucosal leukokeratosis  
Hernandez Fragoso Syndrome 
Histiocytic Dermatoarthritis 
homocystinuria +   
Hyaluronan Metabolism, Defect in 
ichthyosis +   
ichthyosis bullosa of Siemens  
ichthyosis vulgaris +   
Infectious Skin Diseases +   
interstitial keratitis +  
interstitial lung disease +   
Isolated Osteopoikilosis 
Juvenile Spring Eruption of Ears 
juvenile xanthogranuloma 
Keratolytic Winter Erythema 
keratosis +   
keratosis follicularis +   
Keratosis Follicularis Spinulosa Decalvans, X-Linked  
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma  
Kimura disease 
leg dermatosis 
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis 
Lipedema 
lipodystrophy +   
lipoid proteinosis  
lipomatosis +   
localized scleroderma +   
loiasis 
Macroepiphyseal Dysplasia, McAlister Coe Type 
Marden-Walker Syndrome  
Marfan Syndrome, Autosomal Recessive  
MASS Syndrome  
mastocytosis +   
Median Cleft Lip, Corpus Callosum, Lipoma, and Skin Polyps 
mediastinitis +  
Mental Retardation, Joint Hypermobility, and Skin Laxity, with or without Metabolic Abnormalities 
Metabolic Skin Diseases +   
mixed connective tissue disease  
mongolian spot 
monilethrix +   
Morgellons Disease 
mucinoses +   
Muir-Torre syndrome  
multicentric reticulohistiocytosis 
multiple cutaneous and mucosal venous malformations  
Multiple Noduli Cutanei with Urinary Tract Abnormalities 
nail disease +   
necrobiosis lipoidica 
Necrobiotic Disorders +  
Necrolytic Migratory Erythema 
Nephrogenic Fibrosing Dermopathy  
noninfectious dermatoses of eyelid +  
Noonan syndrome +   
ochronosis +  
Oculotrichodysplasia 
orofaciodigital syndrome IX 
ossification of the posterior longitudinal ligament of spine  
Osteopoikilosis +   
otulipenia  
palmoplantar keratosis +   
Papulosquamous Skin Diseases +   
Parana Hard Skin Syndrome 
Pedal Onychogryposis with Keratosis Plantaris and Coarse Hair 
peeling skin syndrome +   
Perifolliculitis Capitis Abscedens Et Suffodiens, Familial 
Peyronie's disease  
photosensitivity disease +   
pigmentation disease +   
plantar fascial fibromatosis 
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  
Prurigo  
Pruritus +   
Pseudoatrophoderma Colli 
pseudoxanthoma elasticum +   
reactive cutaneous fibrous lesion +  
Reticulate Pigmentary Disorder, with Systemic Manifestations  
rheumatic disease +   
rosacea +   
Rothmund-Thomson syndrome +   
Roy Maroteaux Kremp Syndrome 
scalp dermatosis +   
sebaceous gland disease +   
Sjogren-Larsson syndrome +   
Skin Abnormalities +   
skin atrophy 
Skin Fragility-Woolly Hair Syndrome  
Skin Neoplasms +   
skin sarcoidosis 
Stickler syndrome +   
Stiff Skin Syndrome  
Storm Syndrome 
strongyloidiasis  
sweat gland disease +   
synovitis +   
Systemic Hyalinosis  
systemic scleroderma +   
Trichothiodystrophy Syndromes +   
tyrosinemia type II  
Upton Young Syndrome 
urticaria +   
vascular skin disease +   
verruciform xanthoma of skin 
vesiculobullous skin disease +   
Vohwinkel Syndrome, Variant Form  
Volkmann contracture 
Wegener's granulomatosis +   
Weill-Marchesani Syndrome 3  
X-linked ichthyosis +   
xeroderma pigmentosum +   

Synonyms
Exact Synonyms: Dermatolyses ;   Dermatolysis ;   Dermatomegaly ;   loose skin
Narrow Synonyms: CUTIS LAXA, DOMINANT/RECESSIVE
Primary IDs: MESH:D003483
Alternate IDs: RDO:0000088
Definition Sources: MESH:D003483, http://en.wikipedia.org/wiki/Cutis_laxa, http://ghr.nlm.nih.gov/condition/cutis-laxa, https://www.rarediseases.org/rare-disease-information/rare-diseases/byID/175/viewAbstract

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