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Results 1 - 4 of 4 for Thyroid C cell hyperplasia
  1. TSHR gene 
    ... as nonautoimmune autosomal dominant hyperthyroidism (or hereditary toxic thyroid hyperplasia). Sometimes gene mutations are acquired during a person's lifetime and are present only in certain cells. This type of mutation is called somatic, and ...
    https://medlineplus.gov/genetics/gene/tshr - Genetics
  2. Myasthenia gravis 
    ... AUTOIMMUNE MYASTHENIA GRAVIS; MG MYASTHENIA GRAVIS WITH THYMUS HYPERPLASIA PubMed Angelini C. Diagnosis and management of autoimmune myasthenia gravis. Clin ...
    https://medlineplus.gov/genetics/condition/myasthenia-gravis - Genetics
  3. Cowden syndrome 
    ... J, Mester J, Orloff MS, Ringel MD, Eng C. Germline SDHx variants modify breast and thyroid cancer risks in Cowden and Cowden-like syndrome via FAD/NAD-dependant destabilization of p53. Hum Mol Genet. 2012 Jan ... KA, Eng C. Germline mutations and variants in the succinate dehydrogenase ...
    https://medlineplus.gov/genetics/condition/cowden-syndrome - Genetics
  4. GNAS gene 
    ... features depend on the number and location of cells that have the mutated GNAS gene. More About This Health Condition At least two mutations in the GNAS gene have been identified in people with primary macronodular adrenal hyperplasia (PMAH), a disorder that causes multiple lumps (nodules) ...
    https://medlineplus.gov/genetics/gene/gnas - Genetics