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Results 1 - 6 of 6 for Familial 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 gene 
    ... 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 
    ... in neurofibromatosis type 2. These tumors are called meningiomas. Tumors can also occur on other nerves or ... with no history of the disorder in their family.Unlike most other autosomal dominant conditions, in which ...
    https://medlineplus.gov/genetics/condition/neurofibromatosis-type-2 - Genetics
  4. 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
  5. Megalencephaly-capillary malformation syndrome 
    ... noncancerous tumors in the nervous system known as meningiomas). The prevalence of MCAP is unknown. At least ... from a parent and does not run in families. In people with MCAP, a PIK3CA gene mutation ...
    https://medlineplus.gov/...encephaly-capillary-malformation-syndrome - Genetics
  6. ARMC5 gene 
    ... 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