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Ontology Browser

Parent Terms Term With Siblings Child Terms
skin disease +     
Abnormalities, Drug-Induced +   
Abnormalities, Radiation-Induced 
Abnormalities, Severe Teratoid +   
Absence of Nasal Bones 
Absence of Vagina 
Accessory Pancreas 
Achenbach syndrome 
Acneiform Eruptions +   
AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency  
Aicardi syndrome 
allergic cutaneous vasculitis +   
Amastia +   
ancylostomiasis +  
angioedema +   
Atlanto-Axial Fusion 
autoimmune disease of skin and connective tissue +   
Birt-Hogg-Dube syndrome  
Boudhina Yedes Khiari syndrome 
breast disease +   
Bresheck/Bresek Syndrome 
C syndrome  
Cardiovascular Abnormalities +   
Caudal Duplication Anomaly  
cercarial dermatitis 
chancroid +  
chromosomal disease +   
chronic ulcer of skin +   
Complete Absence of Bile and Pancreatic Ducts 
Congenital Aural Atresia  
congenital diaphragmatic hernia +   
Congenital Microtia +   
Congenital Stridor 
contagious pustular dermatitis 
Crane-Heise Syndrome 
Cutaneous Fistula 
cutaneous lupus erythematosus +   
cutis laxa +   
Deal Barratt Dillon Syndrome 
Dermal Fibrosis  
dermatitis +   
dermatomyositis +   
Digestive System Abnormalities +   
Duplication of Eyebrows with Stretchable Skin and Syndactyly 
Ectodermal Dysplasia-Skin Fragility Syndrome  
Eczematous Skin Diseases +   
Elastosis Perforans Serpiginosa 
Elliott Ludman Teebi Syndrome 
endometriosis in scar of skin 
epidermal nevus +   
Erythema +   
erythematosquamous dermatosis 
exanthem +   
Eye Abnormalities +   
eyelid disease +   
FACES Syndrome 
facial dermatosis +   
Facial Ectodermal Dysplasia  
Familial Cryptotia 
filariasis +   
Flynn Aird Syndrome 
Foot Diseases +   
Frank-Ter Haar syndrome  
Gallbladder, Agenesis Of 
Genetic Skin Diseases +   
granulomatosis with polyangiitis +   
hair disease +   
hand dermatosis +  
hemorrhoid +   
Hernandez Fragoso Syndrome 
Hydrocephalus, Skeletal Anomalies, and Mental Disturbance 
ichthyosis +   
Infectious Skin Diseases +   
juvenile xanthogranuloma 
keratosis +   
Kimura disease 
Laryngeal Cleft 
Laryngeal Web, Familial 
leg dermatosis 
lipomatosis +   
localized scleroderma +   
Lymphatic Abnormalities +   
Macroepiphyseal Dysplasia, McAlister Coe Type 
MASS Syndrome  
mastocytosis +   
Mayer-Rokitansky-Kuster-Hauser syndrome +   
Median Cleft Lip, Corpus Callosum, Lipoma, and Skin Polyps 
Mental Retardation, Joint Hypermobility, and Skin Laxity, with or without Metabolic Abnormalities 
Metabolic Skin Diseases +   
Mondini Dysplasia  
mongolian spot 
Morgellons Disease 
multicentric reticulohistiocytosis 
Multiple Abnormalities +   
multiple cutaneous and mucosal venous malformations  
Musculoskeletal Abnormalities +   
nail disease +   
necrobiosis lipoidica 
Necrobiotic Disorders +  
Necrolytic Migratory Erythema 
Nephrogenic Fibrosing Dermopathy  
Nervous System Malformations +   
noninfectious dermatoses of eyelid +  
Pancreas Agenesis, Dorsal 
Papulosquamous Skin Diseases +   
phaeohyphomycosis +  
photosensitivity disease +   
pigmentation disease +   
Pruritus +   
Pseudoatrophoderma Colli 
Pseudopyogenic Granuloma 
reactive cutaneous fibrous lesion +   
Renal and Mullerian Duct Hypoplasia +   
Respiratory System Abnormalities +   
rosacea +   
Roy Maroteaux Kremp Syndrome 
Saito Kuba Tsuruta Syndrome 
scalp dermatosis +   
Schlegelberger Grote Syndrome 
sebaceous gland disease +   
situs inversus +   
Skin Abnormalities +   
Congenital structural abnormalities of the skin.
skin atrophy 
Skin Neoplasms +   
skin sarcoidosis 
Sprengel Deformity 
Stomatognathic System Abnormalities +   
sweat gland disease +   
thyroid malformation +   
tyrosinemia type II  
Upton Young Syndrome 
Urogenital Abnormalities +   
urticaria +   
vascular skin disease +   
verruciform xanthoma of skin 
Vertebral Fusion Posterior Lumbosacral Blepharoptosis 
 acrodermatitis +   
 Anetoderma +   
 Carney complex +   
 ichthyosis +   
 MLS syndrome +   
 Port-Wine Stain +   

Exact Synonyms: Skin Abnormality
Primary IDs: MESH:D012868 ;   RDO:0000167
Definition Sources: MESH:D012868

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