MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, ND: NAMDC terms.
  Most Studied  CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO
Disease Browser
Parent Node:
expandskin disease (MONDO:0005093)
Parent Node:
expandvascular disease (MONDO:0005385)
..Starting node
..expandskin vascular disease ()

       Child Nodes:
........expandangioedema ()
........expandangioma serpiginosum ()
........expandangioosteohypertrophic syndrome ()
........expandataxia - telangiectasia-like disorder ()
........expandataxia telangiectasia ()
........expandBehcet disease ()
........expandblue rubber bleb nevus ()
........expandBockenheimer syndrome ()
........expandcalciphylaxis cutis ()
........expandchilblain lupus ()
........expandCobb syndrome ()
........expandcutaneous collagenous vasculopathy ()
........expandcutis marmorata telangiectatica congenita (disease) ()
........expandFabry disease ()
........expandfamilial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome ()
........expandfamilial multiple nevi flammei ()
........expandgeneralized essential telangiectasia ()
........expandhereditary hemorrhagic telangiectasia ()
........expandlivedo reticularis ()
........expandMaffucci syndrome ()
........expandmalignant atrophic papulosis ()
........expandmegalencephaly-capillary malformation-polymicrogyria syndrome ()
........expandpityriasis lichenoides ()
........expandSneddon syndrome ()
........expandWyburn-Mason syndrome ()



 Sister Nodes: 
..expandangiodysplasia ()
..expandarterial calcification of infancy ()
..expandarterial disorder ()
..expandautosomal recessive cutis laxa type 1 ()
..expandblood vessel neoplasm ()
..expandcalciphylaxis ()
..expandcapillary disease ()
..expandcholesterol embolism ()
..expanddisease of central nervous system or retinal vasculature ()
..expandEhlers-Danlos syndrome, vascular-like type ()
..expandfibrocartilaginous embolism ()
..expandhepatic vascular disease ()
..expandhereditary arterial and articular multiple calcification syndrome ()
..expandischemic colitis ()
..expandischemic disease ()
..expandlethal arteriopathy syndrome due to fibulin-4 deficiency ()
..expandlymphatic vessel neoplasm ()
..expandneurovascular disease ()
..expandnon-inflammatory vasculopathy ()
..expandocular vascular disease ()
..expandperipheral vascular disease ()
..expandrare cause of hypertension ()
..expandrare disease with thoracic aortic aneurysm and aortic dissection ()
..expandskin vascular disease ()
..expandsuperior vena cava syndrome ()
..expandsupine hypotensive syndrome ()
..expandthoracic outlet syndrome ()
..expandthrombotic disease ()
..expandvascular anomaly ()
..expandvascular disorder of penis ()
..expandvascular ectasia ()
..expandvascular hemostatic disease ()
..expandvascular insufficiency disorder ()
..expandvascular occlusion disorder ()
..expandvasculitis ()
..expandvein disease ()
..expandvenous thromboembolism ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:19293
Name:skin vascular disease
Definition:A disease that involves the superficial vasculature.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:disorder of blood vessels affecting skin; skin vascular disorder; superficial vasculature disease; vascular disease of the skin; vascular disorder of skin; vascular disorders of skin; vascular skin disease; vasculature skin disease
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal