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infantile, generalized gm1 gangliosidosis
释义
infantile, generalized GM1 gangliosidosis
in·fan·tile, gen·er·al·ized G
M1
gan·gli·o·si·do·sis
one of the hereditary metabolic diseases of infancy; resembles Tay-Sachs disease, except other organ systems (bone, liver, kidney) are affected.
Synonym(s): familial neuroviscerolipidosis, pseudo-Hurler disease, Type 1 GM1 gangliosidosis
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更新时间:2026/6/30 5:33:48