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neurofibromatosis

The information provided on this page is for informational purposes only. The National Organization for Rare Disorders (NORD) does not endorse the information presented. The content has been gathered in partnership with the MONDO Disease Ontology. Please consult with a healthcare professional for medical advice and treatment.

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Disease Overview

A hereditary neoplastic syndrome in which tumors grow in the nervous system. There are typically 3 main types recognized, but other forms with uncertain etiology exist.

Synonyms

  • Recklinghausen's neurofibromatosis
  • acoustic neurofibromatosis
  • central Neurofibromatosis
  • neurofibromatosis
  • neurofibromatosis syndrome
  • neurofibromatosis type 2
  • neurofibromatosis type 4
  • neurofibromatosis type IV
  • peripheral Neurofibromatosis
  • type IV neurofibromatosis of riccardi
  • von Reklinghausen disease
GARD Disease Summary

The Genetic and Rare Diseases Information Center (GARD) has information and resources for patients, caregivers, and families that may be helpful before and after diagnosis of this condition. GARD is a program of the National Center for Advancing Translational Sciences (NCATS), part of the National Institutes of Health (NIH).

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