CADASIL - CISMeF

Preferred Label : CADASIL;

MeSH definition : A familial, cerebral arteriopathy mapped to chromosome 19q12, and characterized by the presence of granular deposits in small CEREBRAL ARTERIES producing ischemic STROKE; PSEUDOBULBAR PALSY; and multiple subcortical infarcts (CEREBRAL INFARCTION). CADASIL is an acronym for Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy. CADASIL differs from BINSWANGER DISEASE by the presence of MIGRAINE WITH AURA and usually by the lack of history of arterial HYPERTENSION. (From Bradley et al, Neurology in Clinical Practice, 2000, p1146);

MeSH synonym : cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy; dementia, hereditary Multi-Infarct type; dementia, hereditary multi infarct type; cerebral arteriopathy with subcortical infarcts and leukoencephalopathy;

Related MeSH term : CADASILM;

Wikipedia link : https://en.wikipedia.org/wiki/Cerebral arteriopathy with subcortical infarcts and leukoencephalopathy;

Details

Origin ID

D046589;

UMLS CUI

C0751587;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Currated CISMeF NLP mapping
- CADASIL [DO Concept]
- CADASIL [MedDRA Preferred Term]
- CADASIL [Radlex concept]
- CADASIL [MedDRA LLT]
- CADASIL - [cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy] syndrome [ICD-11 Sub-sub category]
- CADASIL 1 [DO Concept]
- CADASIL Syndrome [NCIt concept]
- CADASIL syndrome [PASCAL descriptor]
- Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1 [OMIM Phenotype]
- Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy [MedDRA LLT]
- Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (disorder) [SNOMED CT concept]
- Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy [ORDO Disease]
- cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy [MedDRA Preferred Term]
DO Cross reference
- CADASIL [DO Concept]
Manual NTBT mappings (CISMeF)
- Genetic central nervous system and retinal vascular disease [ORDO Disease]
- Nervous system anomaly with eye involvement [ORDO Disease]
- Rare central nervous system and retinal vascular disease [ORDO Disease]
- Rare cerebrovascular dementia [ORDO Disease]
- Rare dementia [ORDO Disease]
ORDO relation(s)
- Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy [ORDO Disease]
Record concept(s)
- CADASIL [MeSH concept]
- CADASILM [MeSH concept]
Related MeSH Supplementary Concept(s)
- familial vascular leukoencephalopathy [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- CADASIL [MedDRA LLT]
- CADASIL [Radlex concept]
- CADASIL [DO Concept]
- CADASIL [MedDRA Preferred Term]
- CADASIL Syndrome [NCIt concept]
- CADASIL syndrome [PASCAL descriptor]
- CADASIL syndrome [Disease (Nov.)]
- Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1 [OMIM Phenotype]
- Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy [MedDRA LLT]
- Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (disorder) [SNOMED CT concept]
- Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy [ORDO Disease]
- cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy [MedDRA Preferred Term]
Validated automatic mappings to BTNT
- CADASIL syndrome [Disease (Nov.)]

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