선택 - 화살표키/엔터키 닫기 - ESC

 
"neurofibromatosis 2"에 대한 세부 검색 결과입니다
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MeSH(Medical Subject Headings) 맞춤 검색 (http://www.nlm.nih.gov) 결과 : 1 페이지: 1
  • Neurofibromatosis 2 - 새창 An autosomal dominant disorder characterized by a high incidence of bilateral acoustic neuromas as well as schwannomas (NEURILEMMOMA) of other cranial and peripheral nerves, and other benign intracranial tumors including meningiomas, ependymomas, spinal neurofibromas, and gliomas. The disease has been linked to mutations of the NF2 gene (GENES, NEUROFIBROMATOSIS 2) on chromosome 22 (22q12) and usually presents clinically in the first or second decade of life.
    Synonyms : Bilateral Acoustic Neurofibromatosis, Familial Acoustic Neuromas, NF2 (Neurofibromatosis 2), Neurofibromatosis II, Neurofibromatosis Type 2, Neurofibromatosis Type II, Neurofibromatosis, Central NF2, Neurofibromatosis, Central, NF 2, Neurofibromatosis, Type 2
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MeSH(Medical Subject Headings) 유사 검색 (http://www.nlm.nih.gov) 결과 : 0 페이지: 1
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