Disease browser and phenotype portal

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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: Brain Ischemia (D002545)
Parent Node: Cerebrovascular Disorders (D002561)
..Starting node ..Vertebrobasilar Insufficiency (D014715)
Child Nodes:
........Subclavian Steal Syndrome (D013349)
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:	11586
Name:	Vertebrobasilar Insufficiency
Definition:	Localized or diffuse reduction in blood flow through the vertebrobasilar arterial system, which supplies the BRAIN STEM; CEREBELLUM; OCCIPITAL LOBE; medial TEMPORAL LOBE; and THALAMUS. Characteristic clinical features include SYNCOPE; lightheadedness; visual disturbances; and VERTIGO. BRAIN STEM INFARCTIONS or other BRAIN INFARCTION may be associated.
Alternative IDs:
ParentIDs:	MESH:D002545\|MESH:D002561
TreeNumbers:	C10.228.140.300.150.956 \|C14.907.253.092.956 \|C14.907.253.956
Synonyms:	Artery Insufficiencies, Basilar \|Artery Insufficiencies, Vertebral \|Artery Insufficiency, Basilar \|Artery Insufficiency, Vertebral \|Artery Ischemia, Basilar \|Artery Ischemias, Basilar \|Artery Ischemias, Vertebral \|Artery Ischemia, Vertebral \|Artery Stenoses, Bas
Slim Mappings:	Cardiovascular disease\|Nervous system disease
Reference:	MedGen: D014715 MeSH: D014715 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants