Myofibromatosis

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
MYOFIBROMATOSIS, INFANTILE, 1
C4551572228550MONDO:0009227
NOTCH3 Causal — Disgenet
PDGFRB Causal
23731537 28334876 30200486
ClinVar, Disgenet, GenCC, HPO
MYOFIBROMATOSIS, INFANTILE, 2
615293C3809084MONDO:0014122
NOTCH3 Causal
23731542 33509954
ClinVar, Disgenet, HPO
All2 Causal2 Unknown1
Related Diseases Diseases that share the most curated genes with Myofibromatosis.
5 View disease cluster →
Myeloproliferative disease, unclassifiable 1 shared genePDGFRB Related via 1 shared gene including PDGFRB. 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. Acroosteolysis 1 shared genePDGFRB Related via 1 shared gene including PDGFRB. Cerebral arteriopathy with subcortical infarcts and leukoencephalopathy 1 shared geneNOTCH3 Related via 1 shared gene including NOTCH3.