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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 ..Carotid Artery Diseases (D002340)
Child Nodes:
........Carotid Artery Injuries (D020212) 3
........Carotid Artery Thrombosis (D002341)
........Carotid Artery, Internal, Dissection (D020215) 1
........Carotid Stenosis (D016893)
........Carotid-Cavernous Sinus Fistula (D020216)
........Moyamoya Disease (D009072) 4
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:	1787
Name:	Carotid Artery Diseases
Definition:	Pathological conditions involving the CAROTID ARTERIES, including the common, internal, and external carotid arteries. ATHEROSCLEROSIS and TRAUMA are relatively frequent causes of carotid artery pathology.
Alternative IDs:
ParentIDs:	MESH:D002561
TreeNumbers:	C10.228.140.300.200 \|C14.907.253.123
Synonyms:	Arterial Disease, Carotid \|Arterial Diseases, Carotid \|Arterial Diseases, Common Carotid \|Arterial Diseases, External Carotid \|Arterial Diseases, Internal Carotid \|Artery Disease, Carotid \|Artery Diseases, Carotid \|Artery Disorder, Carotid \|Artery Disorders, Car
Slim Mappings:	Cardiovascular disease\|Nervous system disease
Reference:	MedGen: D002340 MeSH: D002340 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants