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Results 1 - 5 of 5 for Familial multiple meningioma
  1. mn1-c-terminal-truncation-syndrome 
    ... impaired intellectual development MCTT syndrome Genetic Testing Registry: Familial meningioma National Organization for Rare Disorders (NORD) CEBALID SYNDROME; ...
    https://medlineplus.gov/.../mn1-c-terminal-truncation-syndrome - Genetics
  2. nf2 
    ... schwannomin Tests of NF2 PubMed MESOTHELIOMA, MALIGNANT; MESOM MENINGIOMA, FAMILIAL, SUSCEPTIBILITY TO NF2, MOESIN-EZRIN-RADIXIN-LIKE (MERLIN) ...
    https://medlineplus.gov/genetics/gene/nf2 - Genetics
  3. neurofibromatosis-type-2 
    ... with no history of the disorder in their family.Unlike most other autosomal dominant conditions, in which ... type 2. BANF Bilateral acoustic neurofibromatosis Central neurofibromatosis Familial acoustic neuromas Neurofibromatosis 2 Neurofibromatosis type 2 merlin ...
    https://medlineplus.gov/genetics/condition/neurofibromatosis-type-2 - Genetics
  4. armc5 
    ... associated with both primary macronodular adrenal hyperplasia and meningioma. J Clin Endocrinol Metab. 2015 Jan;100(1): ... DJ, Scott HS. ARMC5 mutations are common in familial bilateral macronodular adrenal hyperplasia. J Clin Endocrinol Metab. ...
    https://medlineplus.gov/genetics/gene/armc5 - Genetics
  5. primary-macronodular-adrenal-hyperplasia 
    ... associated with both primary macronodular adrenal hyperplasia and meningioma. J Clin Endocrinol Metab. 2015 Jan;100(1): ... DJ, Scott HS. ARMC5 mutations are common in familial bilateral macronodular adrenal hyperplasia. J Clin Endocrinol Metab. ...
    https://medlineplus.gov/.../primary-macronodular-adrenal-hyperplasia - Genetics