cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy 1

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy 1
NOTCH3 Causal — ClinGen
All1 Causal1 Unknown0
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inherited thrombocytopenia 1 shared geneNOTCH3 Related via 1 shared gene including NOTCH3. Myofibromatosis 1 shared geneNOTCH3 Related via 1 shared gene including NOTCH3. Cerebral arteriopathy with subcortical infarcts and leukoencephalopathy 1 shared geneNOTCH3 Related via 1 shared gene including NOTCH3. Cadasil 1 shared geneNOTCH3 Related via 1 shared gene including NOTCH3. Common migraine 1 shared geneNOTCH3 Related via 1 shared gene including NOTCH3.