cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy

Preferred Label : cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy;

CISMeF acronym : CARASIL;

UMLS semantic type : T047 - Disease or Syndrome;

Détails

Origin ID

M0564290;

UMLS CUI

C1838577;

Currated CISMeF NLP mapping
- Autosomal Recessive Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy [NCIt concept]
- CARASIL [Disease (Nov.)]
- CARASIL - [cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy] syndrome [ICD-11 Sub-sub category]
- CARASIL syndrome [MedDRA Preferred Term]
- Cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy [OMIM Phenotype]
- Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy [MedDRA LLT]
- Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (disorder) [SNOMED CT concept]
- Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy [ORDO Disease]
Related record
- cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal Recessive Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy [NCIt concept]
- CARASIL [Disease (Nov.)]
- CARASIL syndrome [MedDRA Preferred Term]
- Cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy [OMIM Phenotype]
- Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy [MedDRA LLT]
- Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (disorder) [SNOMED CT concept]
- Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy [ORDO Disease]

Position du mot-clé dans l'(les) arborescence(s) :

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