3A10.Y
其他特指的遗传性溶血性贫血
Other specified hereditary haemolytic anaemia
- 上级条目
- 3A10 遗传性溶血性贫血
- 层级
- 6 级
索引词 可用于检索该条目的同义词与别名
- 其他特指的遗传性溶血性贫血
- 糖酵解酶紊乱引起的溶血性贫血
- 糖酵解酶紊乱引起的贫血
- 无氧糖酵解紊乱引起的贫血 [possible translation]
- 糖酵解酶缺乏性贫血 [possible translation]
- 无氧糖酵解紊乱伴贫血 [possible translation]
- 无氧糖酵解紊乱引起的贫血
- 糖酵解酶缺乏性贫血
- 无氧糖酵解紊乱伴贫血
- 磷酸丙糖异构酶缺乏引起的溶血性贫血
- 红细胞丙酮酸激酶缺乏性贫血
- 丙酮酸激酶缺乏性贫血
- 丙酮酸激酶缺乏引起的遗传性非球型红细胞溶血性贫血
- 丙酮酸激酶缺乏引起的遗传性溶血性非球细胞性贫血
- 葡萄糖-磷酸异构酶缺乏引起的溶血性贫血
- 葡萄糖磷酸异构酶缺乏引起的溶血性贫血
- 3-磷酸甘油醛脱氢酶缺乏引起的溶血性贫血
- 磷酸甘油醛脱氢酶缺乏引起的贫血
- 甘油醛磷酸脱氢酶缺乏引起的贫血
- 红细胞烯醇化酶缺乏引起的溶血性贫血
- 红细胞烯醇化酶缺乏症
- 红细胞二磷酸甘油酸变位酶缺乏引起的溶血性贫血
- 己糖激酶缺乏引起的非球型红细胞溶血性贫血
- 己糖激酶缺乏性贫血
- 溶血性非球形红细胞遗传性贫血，2型
- 溶血性非球形贫血，2型
- 溶血性非球细胞性贫血，2型
- 腺苷三磷酸酶缺乏引起的溶血性贫血
- 嘧啶5‘核苷酸酶缺乏引起的溶血性贫血
- 尿苷单磷酸水解酶缺乏症
- 腺苷酸激酶缺乏引起的溶血性贫血
- 遗传性球形红细胞增多症
- 先天性溶血性黄疸
- Minkowski-Chauffard综合征
- 先天性球形溶血性贫血
- 先天性球形红细胞增多症
- 家族性球形红细胞增多症
- 球形红细胞性贫血
- （家族性）无胆色素尿性黄疸
- Minkowski-Chauffard病
- 明科斯基-乔福德二氏综合征
- 明科斯基-乔福德二氏病
- 先天性（球形红细胞）溶血性黄疸 [possible translation]
- 无胆色素尿性黄疸 [possible translation]
- 无胆色素尿性黄疸 [possible translation]
- 遗传性球形红细胞性贫血 [possible translation]
- 球形红细胞增多症 [possible translation]
- 无胆色素尿性黄疸
- 无胆色素尿性黄疸
- 球形红细胞增多症
- 遗传性球形红细胞性贫血
- 先天性（球形红细胞）溶血性黄疸
- 东南亚卵圆形红细胞增多症
- 脱水遗传性口形红细胞增多症
- 干瘪细胞增多症
- 脱水遗传性裂口红细胞症
- 遗传性冷水肿细胞增多症，伴stomatin减少
- 遗传性冷水肿细胞增多症
- 中度口形红细胞增多症
- 水化遗传性口形红细胞增多症
- 充水细胞增多症
- Rh缺乏综合征
- Rh-null综合征
- 棘红细胞增多症
- 舞蹈病棘红细胞增多症
- 神经棘红细胞增多症
- Mcleod神经棘红细胞增多综合征
- 遗传性溶血尿毒综合征
- 溶血性-尿毒症综合征不伴有腹泻
- 体质性溶血尿毒综合征
- 非典型溶血尿毒综合征
- 非典型溶血尿毒综合征伴C3异常
- 非典型溶血尿毒综合征伴MCP或CD46异常
- 非典型溶血尿毒综合征伴B因子异常
- 非典型溶血尿毒综合征伴H因子异常
- 非典型溶血尿毒综合征伴I因子异常
- 非典型溶血尿毒综合征伴血栓调节蛋白异常
英文词条（63）
- Other specified hereditary haemolytic anaemia
- Haemolytic anaemias due to disorders of glycolytic enzymes
- anaemia due to anaerobic glycolysis disorder
- anaemia due to disorders of glycolytic enzymes
- anaemia due to glycolytic enzyme deficiency
- glycolysis anaerobic disorder with anaemia
- Haemolytic anaemia due to triose phosphate-isomerase deficiency
- Haemolytic anaemia due to red cell pyruvate kinase deficiency
- hereditary nonspherocytic haemolytic anaemia due to pyruvate kinase deficiency
- pyruvate kinase deficiency anaemia
- Haemolytic anaemia due to glucose-phosphate isomerase deficiency
- Haemolytic anaemia due to glucophosphate isomerase deficiency
- Haemolytic anaemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency
- anaemia due to glyceraldehyde phosphate dehydrogenase deficiency
- Haemolytic anaemia due to red cell enolase deficiency
- Erythrocyte enolase deficiency
- Haemolytic anaemia due to red cell diphosphoglycerate mutase deficiency
- Nonspherocytic haemolytic anaemia due to hexokinase deficiency
- anaemia due to hexokinase deficiency
- Haemolytic nonspherocytic hereditary anaemia, type 2
- haemolytic nonspherocytic anaemia, type 2
- Haemolytic anaemia due to adenosine triphosphatase deficiency
- Haemolytic anaemia due to pyrimidine 5' nucleotidase deficiency
- Uridine monophosphate hydrolase deficiency
- Haemolytic anaemia due to adenylate kinase deficiency
- Hereditary spherocytosis
- Acholuric (familial) jaundice
- Congenital (spherocytic) haemolytic icterus
- Minkowski-Chauffard disease
- Minkowski-Chauffard syndrome
- acholuric icterus
- acholuric jaundice
- anaemia spherocytic
- congenital haemolytic icterus
- congenital spherocytic haemolytic anaemia
- congenital spherocytosis
- familial spherocytosis
- hereditary spherocytic anaemia
- spherocytosis
- Southeast Asian ovalocytosis
- Dehydrated hereditary stomatocytosis
- Xerocytosis
- Hereditary cryohydrocytosis with reduced stomatin
- Hereditary cryohydrocytosis
- Intermediate stomatocytosis syndrome
- Overhydrated hereditary stomatocytosis
- Hydrocytosis
- Rh deficiency syndrome
- Rh-null syndrome
- Acanthocytosis
- Choreoacanthocytosis
- Neuroacanthocytosis
- McLeod neuroacanthocytosis syndrome
- Hereditary haemolytic uraemic syndrome
- Atypical haemolytic uraemic syndrome
- Constitutional haemolytic uraemic syndrome
- Haemolytic-uremic syndrome without diarrhoea
- Atypical haemolytic uraemic syndrome with C3 anomaly
- Atypical haemolytic uraemic syndrome with MCP or CD46 anomaly
- Atypical haemolytic uraemic syndrome with factor B anomaly
- Atypical haemolytic uraemic syndrome with factor H anomaly
- Atypical haemolytic uraemic syndrome with factor I anomaly
- Atypical haemolytic uraemic syndrome with thrombomodulin anomaly
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