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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: Basal Ganglia Diseases (D001480)
Parent Node: Cerebrovascular Disorders (D002561)
..Starting node ..Basal Ganglia Cerebrovascular Disease (D020144)
Child Nodes:
........Basal Ganglia Hemorrhage (D020145) 1
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:	1187
Name:	Basal Ganglia Cerebrovascular Disease
Definition:	A pathological condition caused by impaired blood flow in the basal regions of cerebral hemispheres (BASAL GANGLIA), such as INFARCTION; HEMORRHAGE; or ISCHEMIA in vessels of this brain region including the lateral lenticulostriate arteries. Primary clinical manifestations include involuntary movements (DYSKINESIAS) and muscle weakness (HEMIPARESIS).
Alternative IDs:
ParentIDs:	MESH:D001480\|MESH:D002561
TreeNumbers:	C10.228.140.079.127 \|C10.228.140.300.100 \|C14.907.253.061
Synonyms:	Basal Ganglia Vascular Disease \|Cerebrovascular Disease, Basal Ganglia \|Lenticulostriate Diseases, Vascular \|Lenticulostriate Vascular Disease \|Lenticulostriate Vascular Diseases \|Lenticulostriate Vasculopathies \|Lenticulostriate Vasculopathy \|Vascular Disease,
Slim Mappings:	Cardiovascular disease\|Nervous system disease
Reference:	MedGen: D020144 MeSH: D020144 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants