Disease browser and phenotype portal

Hello! Guest! Please Login or Register! Clinician Mode

Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Cerebrovascular Disorders (D002561)
..Starting node ..Cerebral Small Vessel Diseases (D059345)
Child Nodes:
........CADASIL (D046589) 1
........Cerebral Amyloid Angiopathy, Familial (D028243) 2
........Cerebral Angiopathy, Dysphoric (C565864)
........Fabry Disease (D000795) 2
........MELAS Syndrome (D017241) 1
........Microscopic Polyangiitis (D055953)
........Stroke, Lacunar (D059409)
Sister Nodes:
..Basal Ganglia Cerebrovascular Disease (D020144) 2
..Brain Ischemia (D002545) 16
..Carotid Artery Diseases (D002340) 11
..Cerebral Small Vessel Diseases (D059345) 13
..Cerebrovascular Trauma (D020214) 6
..Dementia, Vascular (D015140) 3
..Intracranial Arterial Diseases (D020765) 35
..Intracranial Arteriovenous Malformations (D002538) 3
..Intracranial Embolism and Thrombosis (D002542) 7
..Intracranial Hemorrhages (D020300) 24
..Leukomalacia, Periventricular (D007969)
..Sneddon Syndrome (D018860)
..Stroke (D020521) 12
..Susac Syndrome (D055955)
..Vascular Headaches (D014653)
..Vasculitis, Central Nervous System (D020293) 7
..Vasospasm, Intracranial (D020301)
..Vertebral Artery Dissection (D020217)
..Vertebrobasilar Insufficiency (D014715) 1
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	1955
Name:	Cerebral Small Vessel Diseases
Definition:	Pathological processes or diseases where cerebral MICROVESSELS show abnormalities. They are often associated with aging, hypertension and risk factors for lacunar infarcts (see LACUNAR INFARCTION); LEUKOARAIOSIS; and CEREBRAL HEMORRHAGE.
Alternative IDs:
ParentIDs:	MESH:D002561
TreeNumbers:	C10.228.140.300.275 \|C14.907.253.329
Synonyms:	Cerebral Microangiopathies \|Cerebral Microangiopathy \|Cerebral Small Vessel Disease \|Microangiopathies, Cerebral \|Microangiopathy, Cerebral
Slim Mappings:	Cardiovascular disease\|Nervous system disease
Reference:	MedGen: D059345 MeSH: D059345 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants