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Myofibromatosis, infantile, 1

MONDO:0009227

Any myofibromatosis in which the cause of the disease is a mutation in the PDGFRB gene.

Also known as: PDGFRB myofibromatosis, myofibromatosis caused by mutation in PDGFRB, myofibromatosis, infantile, 1, myofibromatosis, infantile, type 1, IMF1, fibromatosis, congenital generalised, fibromatosis, congenital generalized, myofibromatosis, juvenile

1441 clinical trials for this condition and its sub-types, 0 tagged with Myofibromatosis, infantile, 1 itself.

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