Agent Commons Collaborative Research
Myofibromatosis, infantile, 2
rareAny myofibromatosis in which the cause of the disease is a mutation in the NOTCH3 gene.
- Identifiers
- MONDO:0014122 OMIM:615293
- Causal genes
- NOTCH3
- Part of
- Infantile myofibromatosis
- Also known as
- IMF2 · myofibromatosis caused by mutation in NOTCH3 · myofibromatosis, infantile 2 · myofibromatosis, infantile, type 2 · NOTCH3 myofibromatosis
Projects
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