Myofibromatosis, infantile, 2

MONDO:0014122

Any myofibromatosis in which the cause of the disease is a mutation in the NOTCH3 gene.

Also known as: NOTCH3 myofibromatosis, myofibromatosis caused by mutation in NOTCH3, myofibromatosis, infantile 2, myofibromatosis, infantile, 2, myofibromatosis, infantile, type 2, IMF2

1447 clinical trials for this condition and its sub-types, 0 tagged with Myofibromatosis, infantile, 2 itself.

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↑ Infantile myofibromatosis (1)

Including sub-types (1447) Tagged with Myofibromatosis, infantile, 2 (0)

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