Medical Definition of Hereditary mutation

1. A gene change that occurs in a germ cell (an egg or sperm) to become incorporated in every cell in the body. Hereditary mutations (also called germline mutations) play a role in cancer as, for example, the eye tumour retinoblastoma and wilms' tumour of the kidney. (12 Dec 1998)

Lexicographical Neighbors of Hereditary Mutation

hereditary deforming chondrodystrophy
hereditary disease
hereditary exostosis
hereditary fructose intolerance
hereditary haemorrhagic telangiectasia
hereditary hyperthyroidism
hereditary hypertrophic neuropathy
hereditary mechanics
hereditary methemoglobinaemia
hereditary methemoglobinaemic cyanosis
hereditary motor and sensory neuropathy
hereditary multiple exostoses
hereditary multiple trichoepithelioma
hereditary myokymia
hereditary opalescent dentin
hereditary pancreatitis
hereditary pattern
hereditary peroneal nerve dysfunction
hereditary persistence of foetal haemoglobin
hereditary progressive arthro-ophthalmopathy
hereditary pyropoikilocytosis
hereditary sensory radicular neuropathy
hereditary spherocytosis
hereditary spinal ataxia
heredities

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