Orphanet: Infantile myofibromatosis

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Infantile myofibromatosis

Disease definition

A rare benign soft tissue tumor characterized by the development of nodules in the skin, striated muscles, bones, and in exceptional cases, visceral organs, leading to a broad spectrum of clinical symptoms. It contains myofibroblasts.


Classification level: Disorder
  • Synonym(s): -
  • Prevalence: Unknown
  • Inheritance: Autosomal dominant or Autosomal recessive or Not applicable 
  • Age of onset: Infancy, Neonatal
  • ICD-10: D48.1
  • OMIM: 228550  615293
  • UMLS: C0432284
  • MeSH: -
  • GARD: 2998
  • MedDRA: -

Detailed information


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