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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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hexafluoride
hexafluoro-2-propanol
hexafluoroacetone
hexafluoroacetylacetonate
hexafluoroisopropanol
hexafluoropropylene
hexafluorosilicic acid
hexafoil
hexagesimal
hexaglot
hexagon
hexagonal
hexagonal boron nitride
hexagonal close packed
hexagonal close-packed structure
hexagonal column
hexagonal crystal system
hexagonal field effect transistor
hexagonal-head bolt
hexagonal lattice
hexagonally
hexagonal method of application
hexagonal nanostructured zeolite particles
hexagonal nipple
hexagonal nut
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更新时间:2026/6/30 6:24:56