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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
genetic disease +     
skin disease +     
Achenbach syndrome 
Acneiform Eruptions +   
adiaspiromycosis 
Adrenocortical Hypofunction, Chronic Primary Congenital 
adrenocorticotropic hormone deficiency  
advanced sleep phase syndrome 3  
age related macular degeneration 8  
Alagille syndrome  
allergic cutaneous vasculitis +   
Alpha-2-Deficient Collagen Disease 
ancylostomiasis +  
angioedema +   
apparent mineralocorticoid excess syndrome  
Aquaporin 1 Deficiency 
aspartylglucosaminuria  
ataxic cerebral palsy 
atrial heart septal defect 3  
atrial heart septal defect 4  
autoimmune disease of skin and connective tissue +   
autoimmune lymphoproliferative syndrome +   
Birt-Hogg-Dube syndrome  
Boudhina Yedes Khiari syndrome 
brachydactyly type A1B 
brachydactyly type A1C  
brachydactyly type A1D  
brachydactyly type B1  
brachydactyly type B2  
brachydactyly type E1  
brachydactyly type E2  
breast disease +   
C syndrome  
CADASIL +   
CAKUT2  
cataract 23  
cataract 25 
cataract 26 multiple types 
cataract 27  
cataract 28 
Cenani-Lenz syndactyly syndrome  
cercarial dermatitis 
chancroid +  
CHARGE syndrome  
chromosomal disease +   
chronic ulcer of skin +   
coenurosis 
complement factor I deficiency  
complex cortical dysplasia with other brain malformations 1  
complex cortical dysplasia with other brain malformations 2  
complex cortical dysplasia with other brain malformations 3  
complex cortical dysplasia with other brain malformations 4  
complex cortical dysplasia with other brain malformations 5  
complex cortical dysplasia with other brain malformations 6  
complex cortical dysplasia with other brain malformations 7  
congenital diarrhea +   
congenital hemolytic anemia +   
Congenital Hepatic Fibrosis  
congenital hypoplastic anemia +   
congenital muscular dystrophy +   
congenital myasthenic syndrome +   
Congenital Pain Insensitivity +   
contagious pustular dermatitis 
Cutaneous Fistula 
cutaneous lupus erythematosus +   
cutis laxa +   
Dermal Fibrosis  
dermatitis +   
Dermatoleukodystrophy 
dermatomyositis +   
desquamative interstitial pneumonia  
dipetalonemiasis 
Duplication of Eyebrows with Stretchable Skin and Syndactyly 
Dwarfism +   
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 +   
eyelid disease +   
FACES Syndrome 
facial dermatosis +   
Facial Ectodermal Dysplasia  
Familial Cirrhosis +   
Familial Dysalbuminemic Hyperthyroxinemia  
Familial Hemophagocytic Lymphohistiocytoses +   
familial hypertrophic cardiomyopathy +   
Familial Lipochrome Histiocytosis 
Familial Mixed Cryoglobulinemia  
Familial Temporal Epilepsy +   
filariasis +   
Flynn Aird Syndrome 
Foot Diseases +   
Frank-Ter Haar syndrome  
frontotemporal dementia and/or amyotrophic lateral sclerosis-3  
frontotemporal dementia and/or amyotrophic lateral sclerosis-4  
Genetic Skin Diseases +   
Diseases of the skin with a genetic component, usually the result of various inborn errors of metabolism.
granulomatosis with polyangiitis +   
hair disease +   
hand dermatosis +  
hemorrhoid +   
hereditary angioedema +   
Hereditary Bilateral Parotidomegaly 
Hereditary Epistaxis 
Hereditary Eye Diseases +   
hereditary lymphedema +   
Hereditary Neoplastic Syndromes +   
Hernandez Fragoso Syndrome 
hypogonadotropic hypogonadism 5 with or without anosmia +   
ichthyosis +   
Infectious Skin Diseases +   
inherited metabolic disorder +   
Isolated Prolactin Deficiency 
juvenile xanthogranuloma 
Kallmann syndrome +   
keratosis +   
Kimura disease 
Laminopathies  
leg dermatosis 
Lennox-Gastaut syndrome  
lipomatosis +   
localized scleroderma +   
loiasis 
Macroepiphyseal Dysplasia, McAlister Coe Type 
Marfan syndrome +   
MASS Syndrome  
mastocytosis +   
Median Cleft Lip, Corpus Callosum, Lipoma, and Skin Polyps 
Mental Retardation, Joint Hypermobility, and Skin Laxity, with or without Metabolic Abnormalities 
Metabolic Skin Diseases +   
mongolian spot  
monogenic disease +   
Morgellons Disease 
multicentric reticulohistiocytosis 
multiple cutaneous and mucosal venous malformations  
nail disease +   
necrobiosis lipoidica 
Necrobiotic Disorders +  
Necrolytic Migratory Erythema 
Nephrogenic Fibrosing Dermopathy  
Nervous System Heredodegenerative Disorders +   
Nonimmune Chronic Idiopathic Neutropenia, Adult  
noninfectious dermatoses of eyelid +  
osteochondrodysplasia +   
otulipenia  
Papulosquamous Skin Diseases +   
phaeohyphomycosis +  
photosensitivity disease +   
pigmentation disease +   
polygenic disease +   
primary hypertrophic osteoarthropathy +   
progressive familial intrahepatic cholestasis +   
Prurigo  
Pruritus +   
Pseudoatrophoderma Colli 
pulmonary alveolar microlithiasis  
reactive cutaneous fibrous lesion +  
rosacea +   
Roy Maroteaux Kremp Syndrome 
Sacral Agenesis with Vertebral Anomalies  
scalp dermatosis +   
sebaceous gland disease +   
Skin Abnormalities +   
skin atrophy 
Skin Neoplasms +   
skin sarcoidosis 
strongyloidiasis  
sweat gland disease +   
tyrosinemia type II  
Upton Young Syndrome 
urticaria +   
vascular skin disease +   
verruciform xanthoma of skin 
vesiculobullous skin disease +   
yellow nail syndrome +  
 Albinism +   
 cherubism +   
 cutis laxa +   
 monilethrix +   
 porokeratosis +   

Synonyms
Exact Synonyms: Genetic Skin Disease
Primary IDs: MESH:D012873
Alternate IDs: RDO:0001013
Definition Sources: MESH:D012873

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.