| mendelian disorder |
a genetic disease, showing a mendelian pattern of inheritance, and caused by a single mutation in the structure of DNA, which causes a single basic defect that has some pathological consequence or consequences. Called also monogenic or single-gene d. See also inborn error of metabolism, under metabolism.
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| Mengo encephalomyelitis |
a type of encephalomyelitis seen in monkeys and mongooses in East Africa, caused by an encephalomyocarditis virus.
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| Mengo virus |
an encephalomyocarditis virus isolated in 1948 in Uganda from a monkey with encephalomyelitis, and later from mosquitoes and a mongoose in the same area; identified also as the cause of an epizootic disease of swine in Panama.
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| mening |
(mening(o)-) [Gr. m[emacr]ninx, gen. m[emacr]ningos membrane] a combining form denoting relationship to a membrane, especially relationship to the meninges.
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| meningioma of the olfactory groove |
a meningioma located in the ethmoid fossa (olfactory groove); symptoms include anosmia, visual defects including Kennedy's syndrome, and psychic disturbances.
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