Myofibromatosis, infantile 2

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Subtype of: Myofibromatosis
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Myofibromatosis, infantile 2
MONDO_0014122
NOTCH3 Unknown
23731542
Open Targets
All1 Causal1 Unknown1
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Inherited thrombocytopenia 1 shared geneNOTCH3 Related via 1 shared gene including NOTCH3. Cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy 1 1 shared geneNOTCH3 Related via 1 shared gene including NOTCH3. Lateral meningocele syndrome 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. Myofibromatosis 1 shared geneNOTCH3 Related via 1 shared gene including NOTCH3.