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bn:01358396n
Noun Concept
Categories: Rare diseases, Dermal and subcutaneous growths
EN
infantile myofibromatosis  Aggressive systemic infantile myofibromatosis  Congenital generalized fibromatosis  Congenital multicentric fibromatosis  Fibromatosis, Congenital Generalized
EN
Infantile myofibromatosis is a rare tumor found in 1 in 150,000 to 1 in 400,000 live births. Wikipedia
Definitions
Relations
Sources
EN
Infantile myofibromatosis is a rare tumor found in 1 in 150,000 to 1 in 400,000 live births. Wikipedia
Connective tissue benign neoplasm that is characterized by the development of benign tumors in the skin, striated muscles, bones, and in exceptional cases, visceral organs Wikidata
IS A
disease
rare disease
GENETIC ASSOCIATION
NOTCH3
PDGFRB
HEALTH SPECIALTY
oncology
Wikipedia
EN
infantile myofibromatosis
Wikidata
EN
infantile myofibromatosis
Wikipedia Redirections
EN
Aggressive systemic infantile myofibromatosis, Congenital generalized fibromatosis, Congenital multicentric fibromatosis, myofibromatosis
Wikidata Alias
EN
Fibromatosis, Congenital Generalized, IMF1, myofibromatosis, MYOFIBROMATOSIS, INFANTILE, 1, MYOFIBROMATOSIS, INFANTILE, 1; IMF1, Myofibromatosis, Infantile, type 1, Myofibromatosis, Juvenile

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