Myofibromatosis, Infantile, 1 (IMF1)

Myofibromatosis, Infantile, 1(来自ICD-11)

别称:

Congenital Generalized Fibromatosis

Imf1

Cgf

Fibromatosis, Congenital Generalized

Myofibromatosis, Infantile, Type 1

Myofibromatosis, Infantile 1

Myofibromatosis, Juvenile

Infantile Myofibromatosis

Juvenile Myofibromatosis

Myofibromatosis

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Myofibromatosis, Infantile, 1, also known as congenital generalized fibromatosis, is related to fibromatosis and peroxisome biogenesis disorder 5a. An important gene associated with Myofibromatosis, Infantile, 1 is PDGFRB (Platelet Derived Growth Factor Receptor Beta). Affiliated tissues include skin and skeletal muscle, and related phenotypes are fibroma and myofibromatosis

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