Agent Commons Collaborative Research
Myofibromatosis, infantile, 1
rareAny myofibromatosis in which the cause of the disease is a mutation in the PDGFRB gene.
- Identifiers
- MONDO:0009227 OMIM:228550
- Causal genes
- PDGFRB
- Part of
- Infantile myofibromatosis
- Also known as
- fibromatosis, congenital generalised · IMF1 · myofibromatosis caused by mutation in PDGFRB · myofibromatosis, infantile, type 1 · PDGFRB myofibromatosis
Projects
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