loading...| Preferred Name |
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy |
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| Synonyms |
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| ID |
http://www.semanticweb.org/ontologies/STO.owl#OWLClass_34916cb4_1d91_4f55_9517_43c81ba47005 |
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| hasDbXref |
MIM: 125310 |
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| isDefinedBy |
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a rare autosomal dominant, adult-onset inherited cerebral vascular disease, characterized by migraines, recurrent transient ischemic attacks, and strokes leading to cognitive decline and dementia. cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is due to mutations in the NOTCH3 gene. |
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| label |
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy |
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| prefixIRI |
OWLClass_34916cb4_1d91_4f55_9517_43c81ba47005 |
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| prefLabel |
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy |
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| references |
Gorelick, P. B., & Alter, M. (2002). The prevention of stroke. Peterson's. Eastvold, A., & Suchy, Y. (2011). Cadasil. In Encyclopedia of Clinical Neuropsychology (pp. 469-470). Springer New York. |
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| source |
Merritt, H. H. (2010). Merritt's neurology. L. P. Rowland, & T. A. Pedley (Eds.). Lippincott Williams & Wilkins. |
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| synonyms |
CADASIL |
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| subClassOf |
http://www.semanticweb.org/ontologies/STO.owl#OWLClass_f1b6be78_9d07_42df_8fa2_fd57559fec3e |