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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: Cerebrovascular Disorders (D002561)
..Starting node ..Vasospasm, Intracranial (D020301)
Child Nodes:
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:	11544
Name:	Vasospasm, Intracranial
Definition:	Constriction of arteries in the SKULL due to sudden, sharp, and often persistent smooth muscle contraction in blood vessels. Intracranial vasospasm results in reduced vessel lumen caliber, restricted blood flow to the brain, and BRAIN ISCHEMIA that may lead to hypoxic-ischemic brain injury (HYPOXIA-ISCHEMIA, BRAIN).
Alternative IDs:
ParentIDs:	MESH:D002561
TreeNumbers:	C10.228.140.300.900 \|C14.907.253.951
Synonyms:	Angiospasm, Cerebral \|Angiospasm, Intracranial \|Angiospasms, Cerebral \|Angiospasms, Intracranial \|Artery Spasm, Cerebral \|Artery Spasms, Cerebral \|Cerebral Angiospasm \|Cerebral Angiospasms \|Cerebral Artery Spasm \|Cerebral Artery Spasms \|Cerebral Vasospasm \|Cerebral
Slim Mappings:	Cardiovascular disease\|Nervous system disease
Reference:	MedGen: D020301 MeSH: D020301 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants