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均染区 相关科技名词
- 黏多糖贮积症IH型mucopolysaccharidosis type IH;Hurler syndrome
- 黏多糖贮积症IS型mucopolysaccharidosis type IS;Scheie syndrome
- 黏多糖贮积症Ⅱ型mucopolysaccharidosis type Ⅱ;Hunter syndrome
- 黏多糖贮积症Ⅲ型mucopolysaccharidosis type Ⅲ;Sanfilippo syndrome
- 黏多糖贮积症ⅢA型mucopolysaccharidosis type ⅢA
- 黏多糖贮积症ⅢB型mucopolysaccharidosis type ⅢB
- 黏多糖贮积症ⅢC型mucopolysaccharidosis type ⅢC
- 黏多糖贮积症ⅢD型mucopolysaccharidosis type ⅢD
- 黏多糖贮积症Ⅳ型mucopolysaccharidosis typeⅣ;Morquio syndrome
- 黏多糖贮积症ⅣA型mucopolysaccharidosis type ⅣA
- 黏多糖贮积症ⅣB型mucopolysaccharidosis type ⅣB
- 黏多糖贮积症Ⅵ型mucopolysaccharidosis type Ⅵ;Maroteaux-Lamy syndrome
- 黏多糖贮积症Ⅶ型mucopolysaccharidosis type Ⅶ;Sly syndrome
- 黏脂贮积症Ⅱ型mucolipidosis type Ⅱ
- 黏脂贮积症Ⅲ型mucolipidosis type Ⅲ;pseudo- Hurler polydystrophy
- 甘露糖苷贮积症mannosidosis
- 岩藻糖苷贮积症fucosidosis
- 涎酸贮积症sialidosis
- 神经鞘脂贮积症sphingolipidosis
- GM1神经节苷脂贮积症GM1 gangliosidosis
- GM2神经节苷脂贮积症变异型BGM2 gangliosidosis variant B
- GM2神经节苷脂贮积症变异型OGM2 gangliosidosis variant O;Sandhoff disease
- 异染性脑白质营养不良metachromatic leukodystrophy
- 多种硫酸酯酶缺乏症multiple sulfatase deficiency
- 球形细胞脑白质营养不良globoid cell leukodystrophy
- 酸性脂酶缺乏症acid lipase deficiency;Wolman disease
- 甲状腺素结合球蛋白缺乏症thyroxine-binding globulin defi- ciency;TBG deficiency
- 睾丸女性化testicular feminization
- 类固醇5α-还原酶缺乏症steroid 5α-reductase deficiency
- 类固醇硫酸酯酶缺乏症steroid sulfatase deficiency
- 假性甲状旁腺功能减退症pseudohypoparathyroidism
- 类固醇21-羟化酶缺乏症steroid 21-hydroxylase deficiency;congenital adrenal hyperplasia
- 家族性低磷酸血症佝偻病familial hypophosphatemic rickets
- 低磷酸血症骨病hypophosphatemic bone disease
- 维生素D依赖性佝偻病Ⅰ型Vitamin D dependent rickets type Ⅰ
- 维生素D依赖性佝偻病Ⅱ型Vitamin D dependent rickets type Ⅱ
- 葡萄糖-6-磷酸脱氢酶缺乏症glucose-6-phosphate dehydroge- nase deficiency
- 生物素酰胺酶缺乏症biotinidase deficiency
- α-珠蛋白生成障碍性贫血α-thalassemia
- β-珠蛋白生成障碍性贫血β-thalassemia
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