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Syndromic disease
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Cerebral arteriopathy with subcortical infarcts and leukoencephalopathy
Cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy 1
rare
Identifiers
MONDO:0979867
OMIM:621295
Causal genes
NOTCH3
Part of
Autosomal recessive disease
Cerebral arteriopathy with subcortical infarcts and leukoencephalopathy
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