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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: Arterial Occlusive Diseases (D001157)
Parent Node: Carotid Artery Diseases (D002340)
..Starting node ..Carotid Stenosis (D016893)
Child Nodes:
Sister 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
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	1795
Name:	Carotid Stenosis
Definition:	Narrowing or stricture of any part of the CAROTID ARTERIES, most often due to atherosclerotic plaque formation. Ulcerations may form in atherosclerotic plaques and induce THROMBUS formation. Platelet or cholesterol emboli may arise from stenotic carotid lesions and induce a TRANSIENT ISCHEMIC ATTACK; CEREBROVASCULAR ACCIDENT; or temporary blindness (AMAUROSIS FUGAX). (From Adams et al., Principles of Neurology, 6th ed, pp822-3)
Alternative IDs:
ParentIDs:	MESH:D001157\|MESH:D002340
TreeNumbers:	C10.228.140.300.200.360 \|C14.907.137.230 \|C14.907.253.123.360
Synonyms:	Artery Narrowing, Carotid \|Artery Narrowings, Carotid \|Artery Plaque, Carotid \|Artery Plaques, Carotid \|Artery Stenoses, Carotid \|Artery Stenosis, Carotid \|Carotid Artery Narrowing \|Carotid Artery Narrowings \|Carotid Artery Plaque \|Carotid Artery Plaques \|Carotid
Slim Mappings:	Cardiovascular disease\|Nervous system disease
Reference:	MedGen: D016893 MeSH: D016893 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants