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Medical Definition of Infantile generalised GM1 gangliosidosis
1. One of the hereditary metabolic diseases of infancy; resembles Tay-Sachs disease, except other organ systems (bone, liver, kidney) are affected. Synonym: familial neuroviscerolipidosis, pseudo-Hurler disease, Type 1 GM1 gangliosidosis. (05 Mar 2000)
Lexicographical Neighbors of Infantile Generalised GM1 Gangliosidosis
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