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:
expandnervous system disorder (MONDO:0005071)
Parent Node:
expandvascular disease (MONDO:0005385)
..Starting node
..expandneurovascular disease ()

       Child Nodes:
........expandataxia - telangiectasia-like disorder ()
........expandataxia telangiectasia ()
........expandBannayan-Riley-Ruvalcaba syndrome ()
........expandbasal laminar drusen ()
........expandbenign choroid plexus neoplasm ()
........expandbenign neoplasm of choroid ()
........expandcampomelia, Cumming type ()
........expandcarotid body paraganglioma ()
........expandcavernous sinus meningioma ()
........expandcentral areolar choroidal dystrophy ()
........expandcentral nervous system angiosarcoma ()
........expandcentral nervous system hemangioma ()
........expandcentral nervous system vasculitis ()
........expandcerebral sinovenous thrombosis ()
........expandcerebral visual impairment ()
........expandcerebrovascular disorder ()
........expandChar syndrome ()
........expandchoroid cancer ()
........expandchoroid plexus cancer ()
........expandchoroidal sclerosis ()
........expandchoroideremia ()
........expandCryoglobulinemic vasculitis ()
........expanddeafness-lymphedema-leukemia syndrome ()
........expandeosinophilic granulomatosis with polyangiitis ()
........expanderythromelalgia ()
........expandeyelid capillary hemangioma ()
........expandFabry disease ()
........expandgenetic central nervous system and retinal vascular disease ()
........expandgyrate atrophy ()
........expandhemangioblastoma ()
........expandhemangioma of retina ()
........expandHennekam syndrome ()
........expandhypercoagulability syndrome due to glycosylphosphatidylinositol deficiency ()
........expandintracranial hypertension ()
........expandjugulotympanic paraganglioma ()
........expandmacrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome ()
........expandmedian arcuate ligament syndrome ()
........expandMeige disease ()
........expandmicrocephaly with or without chorioretinopathy, lymphedema, or mental retardation ()
........expandmicrocephaly-capillary malformation syndrome ()
........expandmicroscopic polyangiitis ()
........expandmigraine disorder ()
........expandneoplasm of aortic body ()
........expandneurofibromatosis type 1 ()
........expandNorman-Roberts syndrome ()
........expandparagangliomas 1 ()
........expandparagangliomas 2 ()
........expandparagangliomas 3 ()
........expandparagangliomas 4 ()
........expandparagangliomas 5 ()
........expandPEHO syndrome ()
........expandpelvis syndrome ()
........expandpolyarteritis nodosa ()
........expandprolidase deficiency ()
........expandProteus syndrome ()
........expandretinal dystrophies primarily involving Bruch's membrane ()
........expandretinal ischemia ()
........expandretinal vascular disease ()
........expandsimple cryoglobulinemia ()
........expandsporadic pheochromocytoma/secreting paraganglioma ()
........expandSturge-Weber syndrome ()
........expandsubarachnoid hemorrhage (disease) ()
........expandtrigeminal autonomic cephalalgia ()
........expandWilliams 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:43218
Name:neurovascular disease
Definition:A disorder of the nervous system related to a vascular etiology.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:disease of nervous system vasculature; nervous system disorder of vasculature; neurovascular disorder; vasculature nervous system disorder
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal