Medical Definition of Gangliosidosis g(m1)

1. Form of gangliosidosis characterised by accumulation of g(m1) ganglioside and oligosaccharides, and caused by an absence or severe deficiency of beta-galactosidase a. The three phenotypes of g(m1) gangliosidosis are called infantile (generalised), juvenile, and adult (types 1, 2, and 3 respectively), referring to the age at which clinical manifestations appear. (12 Dec 1998)

Lexicographical Neighbors of Gangliosidosis G(m1)

ganglion terminale
ganglion trigeminale
ganglion tympanicum
ganglion vertebrale
ganglion vestibulare
ganglioplegic
gangliosialidosis
ganglioside
ganglioside
gangliosides
ganglioside galactosyltransferase
ganglioside lipidosis
ganglioside O-acetyltransferase
gangliosidoses
gangliosidosis
gangliosidosis g(m1) (current term)
gangly
gangosa
gangplank
gangplanks
gangplow
gangplows
gangrel
gangrels
gangrene
gangrene
gangrened
gangrenes
gangrening
gangrenous

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