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A genetic condition in which tumors form on the nerves of the inner ear and cause loss of hearing and balance. Tumors may also occur in the brain and on nerves in the skull and spinal cord, and may cause loss of speech, eye movement, and the ability to swallow.

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Data Correlations | 1 study

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Genes category icon Genes
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NF2 100 100
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Biogroups category icon Biogroups
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FERM, 3-helical bundle 100 100
FERM/acyl-CoA-binding protein, 3-he… 100 100
Band 4.1, N-terminal 100 100
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Individual Studies

  • OMIM - Congenital disorder

    Homo sapiens Homo sapiens | Mutations/Phenotypic   Mutations/Phenotypic

    This study contains curated human phenotype data extracted from OMIM. Additional computational processing and curation of the phenotype data was performed to further organize and group data from related phenotypes into unifying disease categories.

    Source: NextBio Library/Mutation and Phenotypic data
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Associated Researchers

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Thought leaders and organizations working on research involving neurofibromatosis type 2.

View All Author iconAuthors
  • Marco Giovannini
  • Mia Maccollin
  • Michael J Link
  • Xandra O Breakefield
  • J Zucman-Rossi
View All Clinical trial sponsors icon Clinical Trials Sponsors
  • National Cancer Institute (NCI)
  • FDA Office of Orphan Products Development
  • University of Alabama at Birmingham
  • Mayo Clinic
  • Memorial Sloan-Kettering Cancer Center
View All Affiliations icon Organizations
  • Massachusetts General Hospital
  • Mayo Clinic
  • St Mary's Hospital
  • John Radcliffe Hospital
  • National Institute of Neurological Disorders and Stroke

Clinical Trials | 64 trials

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News | 12 stories

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Community

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