hexosaminidase单词基本解析：

n.己糖胺酶，氨基己糖苷酶
n. [生化]己糖胺酶, 氨基己糖苷酶
n.己糖胺酶，氨基己糖苷酶；

hexosaminidase变化用词：

hexosaminidase英英释义：

HexosaminidaseHexosaminidase (, beta-acetylaminodeoxyhexosidase, N-acetyl-beta-D-hexosaminidase, N-acetyl-beta-hexosaminidase, N-acetyl hexosaminidase, beta-hexosaminidase, beta-acetylhexosaminidinase, beta-D-N-acetylhexosaminidase, beta-N-acetyl-D-hexosaminidase, beta-N-acetylglucosaminidase, hexosaminidase A, N-acetylhexosaminidase, beta-D-hexosaminidase) is an enzyme involved in the hydrolysis of terminal N-acetyl-D-hexosamine residues in N-acetyl-β-D-hexosaminides.

以上来源于:Wikipedia

hexosaminidase中文词源：

hexosaminidase用法和例句：

hexosaminidase

N-acetyl hexosaminidase

N-乙酰氨基己糖苷酶

acetyl hexosaminidase

乙酰氨基己糖苷酶

hexosaminidase A

己糖胺酶A

Hexosaminidase A and B deficiency

己糖胺酶A和B缺乏

Hexosaminidase activator deficiency

己糖胺酶激活因子缺乏

Sandhoff results from a genetic mutation that reduces the body's supply of an enzyme, called hexosaminidase ("hex"), used by brain cells to metabolize excess fatty material called lipids.

由基因突变导致的山德霍夫氏病会减少体内的一种叫做己糖胺酶的供应，而脑细胞用它来代谢过多的脂质。

Severe hexosaminidase A deficiency

重度己糖胺酶A缺乏

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