cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2
human disease
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cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2
Summary
cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2 is a rare disease[1].
Key Facts
- cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2's instance of is recorded as rare disease[2].
- cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2's instance of is recorded as class of disease[3].
- cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2's subclass of is recorded as CADASIL[4].
- cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2's subclass of is recorded as autosomal dominant disease[5].
- cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2's OMIM ID is recorded as 616779[6].
- cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2's Disease Ontology ID is recorded as DOID:0111036[7].
- cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2's genetic association is recorded as HTRA1[8].
- cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111036[9].
- cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2's exact match is recorded as http://identifiers.org/doid/DOID:0111036[10].
- cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2's UMLS CUI is recorded as C4225211[11].
- cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2's ICD-10-CM is recorded as F01.1[12].
- cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2's Mondo ID is recorded as MONDO_0014768[14].
- cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2's UniProt disease ID is recorded as DI-04641[15].