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Ontology Browser

Parent Terms Term With Siblings Child Terms
acrodermatitis +   
Alpha-2-Deficient Collagen Disease 
Anetoderma +   
Benign DERMATOSIS caused by a loss of dermal ELASTIC TISSUE resulting in localized sac-like areas of flaccid skin. It can be either primary (idiopathic) or secondary to other skin conditions, PENICILLAMINE use, or premature birth.
arterial tortuosity syndrome  
Au-Kline Syndrome  
autoimmune disease of skin and connective tissue +   
Autoinflammation with Arthritis and Dyskeratosis  
Barber-Say syndrome  
Beare-Stevenson cutis gyrata syndrome  
Blepharophimosis with Ptosis, Syndactyly, and Short Stature 
blepharophimosis, ptosis, and epicanthus inversus syndrome +   
Bloch-Sulzberger syndrome +   
bone disease +   
Bone Fragility with Contractures, Arterial Rupture, and Deafness  
Book Syndrome 
bullous skin disease +   
C1q Deficiency  
Carney complex +   
cartilage disease +   
cellulitis +   
chronic interstitial cystitis 
collagen disease +   
Congenital Fascial Dystrophy 
congenital vertical talus  
Connective Tissue Neoplasms +   
contractures, pterygia, and spondylocarpotarsal fusion syndrome +   
Cutaneous Hemangiomatosis with Associated Features 
cutaneous lupus erythematosus +   
cutis laxa +   
dental pulp disease +   
Dermal Ridges, Nelson Syndrome 
dermatomyositis +   
Dupuytren Contracture +  
dyskeratosis congenita +   
ectodermal dysplasia +   
Ehlers-Danlos syndrome +   
enthesopathy +  
epidermolysis bullosa +   
Epithelial Squamous Dysplasia, Keratinizing Desquamative, of Urinary Tract 
Erosive Arthropathy 
Familial Dyskeratotic Comedones 
Familial Popliteal Pterygium Syndrome 
fasciitis +   
fetal encasement syndrome  
fibrodysplasia ossificans progressiva  
Ganglion Cysts 
Hairy Palms and Soles 
Hereditary Benign Intraepithelial Dyskeratosis 
Hereditary Sclerosing Poikiloderma +   
homocystinuria +   
hyaline fibromatosis syndrome  
Hyperkeratotic Cutaneous Capillary-Venous Malformations Associated with Cerebral Capillary Malformations  
Hypohidrosis with Abnormal Palmar Dermal Ridges 
ichthyosis +   
Ichthyosis-Mental Retardation Syndrome with Large Keratohyalin Granules in the Skin 
Infantile Cataract, Skin Abnormalities, Glutamate Excess, and Impaired Intellectual Development  
Inflammatory Poikiloderma with Hair Abnormalities and Acral Keratoses  
interstitial keratitis +  
interstitial lung disease +   
Isolated Pterygium Colli 
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma  
lethal restrictive dermopathy  
lipodystrophy +   
Marden-Walker Syndrome  
mediastinitis +  
MLS syndrome +   
mucinoses +   
multiple benign circumferential skin creases on limbs +   
Multiple Self-healing Palmoplantar Carcinoma  
Neurodevelopmental Disorder with Hypotonia, Dysmorphic Facies, and Skin Abnormalities  
Noonan syndrome +   
ochronosis +   
Oculocerebrocutaneous Syndrome 
Osteopoikilosis +   
Patternless Dermal Ridges 
Peyronie's disease  
plantar fascial fibromatosis 
poikiloderma with neutropenia  
Port-Wine Stain +   
prolidase deficiency  
pseudoxanthoma elasticum +   
rheumatic disease +   
Ridges-off-the-end Syndrome 
Rothmund-Thomson syndrome +   
Sclerema Neonatorum 
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, 3  
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  
Stickler syndrome +   
synovitis +   
systemic lupus erythematosus +   
trichothiodystrophy +   
Urban Schosser Spohn Syndrome  
Vascular Hyalinosis 
VISS syndrome  
Volkmann contracture 
Winter Shortland Temple Syndrome  
xeroderma pigmentosum +   

Exact Synonyms: Anetodermas ;   Primary Anetoderma ;   Primary Anetodermas ;   Secondary Anetoderma ;   Secondary Anetodermas
Primary IDs: MESH:D057088
Xrefs: NCI:C133885
Definition Sources: MESH:D057088

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