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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 ..Stroke (D020521)
Child Nodes:
........Brain Infarction (D020520) 10
........Stroke, Lacunar (D059409)
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:	10708
Name:	Stroke
Definition:	A group of pathological conditions characterized by sudden, non-convulsive loss of neurological function due to BRAIN ISCHEMIA or INTRACRANIAL HEMORRHAGES. Stroke is classified by the type of tissue NECROSIS, such as the anatomic location, vasculature involved, etiology, age of the affected individual, and hemorrhagic vs. non-hemorrhagic nature. (From Adams et al., Principles of Neurology, 6th ed, pp777-810)
Alternative IDs:	OMIM:606799
ParentIDs:	MESH:D002561
TreeNumbers:	C10.228.140.300.775 \|C14.907.253.855
Synonyms:	Acute Cerebrovascular Accident \|Acute Cerebrovascular Accidents \|Acute Stroke \|Acute Strokes \|Apoplexy \|Apoplexy, Cerebrovascular \|Brain Vascular Accident \|Brain Vascular Accidents \|Cerebral Stroke \|Cerebral Strokes \|Cerebrovascular Accident \|Cerebrovascular Accide
Slim Mappings:	Cardiovascular disease\|Nervous system disease
Reference:	MedGen: D020521 MeSH: D020521 OMIM: 606799; Genes: PDE4D;
Phenotypes
Disease Causing ClinVar Variants