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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  
allergic cutaneous vasculitis +   
Alpha-2-Deficient Collagen Disease 
ancylostomiasis +  
angioedema +   
Aquaporin 1 Deficiency 
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  
BOCKENHEIMER 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 25 
cataract 26 multiple types 
cataract 27  
cataract 28 
Cenani-Lenz syndactyly syndrome  
cercarial dermatitis 
chancroid +  
chromosomal disease +   
chronic ulcer of skin +   
coenurosis 
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  
Congenital Hepatic Fibrosis  
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 +   
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 Bilateral Parotidomegaly 
Hereditary Epistaxis 
Hereditary Eye Diseases +   
hereditary lymphedema +   
Hereditary Neoplastic Syndromes +   
Hernandez Fragoso Syndrome 
hypogonadotropic hypogonadism 5 with or without anosmia +   
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 +   
Papulosquamous Skin Diseases +   
phaeohyphomycosis +  
photosensitivity disease +   
pigmentation disease +   
polygenic disease +   
primary hypertrophic osteoarthropathy +   
progressive familial intrahepatic cholestasis +   
Prurigo  
Pruritus +   
Pseudoatrophoderma Colli 
Pseudopyogenic Granuloma 
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 
sweat gland disease +   
tyrosinemia type II  
Upton Young Syndrome 
vascular skin disease +   
verruciform xanthoma of skin 
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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