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Ontology Browser

Parent Terms Term With Siblings Child Terms
genetic disease +     
skin disease +     
Achenbach syndrome 
Acneiform Eruptions +   
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 +  
anemia +   
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  
blood coagulation disease +   
blood group incompatibility +   
blood protein disease +   
This is a very rare condition characterized by extensive, circumscribed venous malformations (phlebectasias) involving all veins, including the smallest ones, on the arms and legs. It is present at birth (congenital) and is progressive during life. The venous dilatation can be seen beneath the skin on the arms and legs. It may occur on one or both sides.
bone marrow disease +   
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  
cataract 25 
cataract 26 multiple types 
cataract 27  
cataract 28 
Cenani-Lenz syndactyly syndrome  
cercarial dermatitis 
chancroid +  
chromosomal disease +   
chronic ulcer of skin +   
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 +   
dermatomyositis +   
desquamative interstitial pneumonia  
Duplication of Eyebrows with Stretchable Skin and Syndactyly 
Dwarfism +   
Ectodermal Dysplasia-Skin Fragility Syndrome  
Eczematous Skin Diseases +   
Elastosis Perforans Serpiginosa 
Elevated Adenosine Triphosphate of Erythrocytes  
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 Macrocytosis  
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 +   
granulomatosis with polyangiitis +   
hair disease +   
hand dermatosis +  
Hematologic Neoplasms +   
Hematologic Pregnancy Complications 
hemorrhoid +   
Hereditary Bilateral Parotidomegaly 
Hereditary Epistaxis 
Hereditary Eye Diseases +   
hereditary lymphedema +   
Hereditary Neoplastic Syndromes +   
Hernandez Fragoso Syndrome 
Infectious Skin Diseases +   
inherited metabolic disorder +   
Isolated Prolactin Deficiency 
juvenile xanthogranuloma 
Kabuki syndrome +   
Kallmann syndrome +   
keratosis +   
Kimura disease 
Laminopathies +   
leg dermatosis 
leukocyte disease +   
lipomatosis +   
localized scleroderma +   
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 +   
pancytopenia +   
Papulosquamous Skin Diseases +   
phaeohyphomycosis +  
photosensitivity disease +   
pigmentation disease +   
polyagglutination +   
polycythemia +   
polygenic disease +   
primary hypertrophic osteoarthropathy +   
progressive familial intrahepatic cholestasis +   
Pruritus +   
Pseudoatrophoderma Colli 
Pseudopyogenic Granuloma 
reactive cutaneous fibrous lesion +   
Rh isoimmunization  
rosacea +   
Roy Maroteaux Kremp Syndrome 
Sacral Agenesis with Vertebral Anomalies  
scalp dermatosis +   
sebaceous gland disease +   
Skin Abnormalities +   
skin atrophy 
Skin Neoplasms +   
skin sarcoidosis 
sulfhemoglobinemia +  
sweat gland disease +   
Tn polyagglutination syndrome  
Transfusion Reaction +   
tyrosinemia type II  
Upton Young Syndrome 
vascular skin disease +   
verruciform xanthoma of skin 
yellow nail syndrome +  

Exact Synonyms: genuine diffuse phlebectasia
Primary IDs: ORPHA:217008
Definition Sources:, ORPHA:217008

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