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bn:00571082n
Noun Concept
Categories: Cerebrovascular diseases, Skin conditions resulting from errors in metabolism, Deficiencies of intracellular signaling peptides and proteins, Syndromes
EN
CADASIL syndrome  CADASIL  cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy  Autosomal dominant cerebral artery disease  Autosomal dominant cerebral artery disease with subcortical infarct and leukoencephalopathy
EN
CADASIL or CADASIL syndrome, involving cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, is the most common form of hereditary stroke disorder, and is thought to be caused by mutations of the Notch 3 gene on chromosome 19. Wikipedia
Definitions
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Sources
EN
CADASIL or CADASIL syndrome, involving cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, is the most common form of hereditary stroke disorder, and is thought to be caused by mutations of the Notch 3 gene on chromosome 19. Wikipedia
Autosomal dominant cerebrovascular disorder characterized by recurrent subcortical ischemic stroke and cognitive impairment Wikidata
IS A
rare disease
leukodystrophy
GENETIC ASSOCIATION
NOTCH3
HTRA1
HAS CAUSE
mutation
HEALTH SPECIALTY
cardiology
neurology
medical genetics
MEDICAL EXAMINATIONS
medical history
genetic screening
magnetic resonance imaging
POSSIBLE TREATMENT
lipid-lowering medicine
antiplatelet drug
SYMPTOMS
stroke
headache
dementia
Wikipedia
EN
CADASIL syndrome
Wikidata
EN
CADASIL
Wikipedia Redirections
EN
CADASIL, Cerebral arteriopathy with subcortical infarcts and leukoencephalopathy, Cerebral Autosomal Dominant Arteriopathy Subcortical Infarcts and Leukoencephalopathy, cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy syndrome, Cerebral autosomal dominant ateriopathy with subcortical infarcts and leukoencephalopathy
Wikidata Alias
EN
Autosomal dominant cerebral artery disease, Autosomal dominant cerebral artery disease with subcortical infarct and leukoencephalopathy, CADASIL Syndrome, Casil, CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY; CADASIL, Cerebral Autosomal-Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy, cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, Dementia, Hereditary Multi-Infarct Type, hereditary multi-infarct dementia

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