3A01.0
遗传性维生素B12缺乏性贫血
Hereditary vitamin B12 deficiency anaemia
- 层级
- 5 级
定义
这是一种遗传性维生素B12低水平血症。如果长时间不治疗，会对神经组织造成永久性损害。维生素B12是通过对恶性贫血的调查而发现的，恶性贫血是一种自身免疫性疾病，破坏胃分泌内在因子的壁细胞。
This is a hereditary low blood level of vitamin B12. It can cause permanent damage to nervous tissue if left untreated long enough. Vitamin B12 itself was discovered through investigation of pernicious anaemia, which is an autoimmune disease that destroys parietal cells in the stomach that secrete intrinsic factor.
索引词 可用于检索该条目的同义词与别名
- 遗传性维生素B12缺乏性贫血
- 遗传性维生素B12缺乏引起的巨幼细胞性贫血
- 氰钴胺素代谢缺陷
- 先天性内因子缺乏 [possible translation]
- 先天性内因子缺乏
- 钴转运蛋白缺乏引起遗传性巨幼细胞性贫血
- 钴转运蛋白II缺乏引起的先天性巨幼细胞性贫血
- TCN2[钴转运蛋白II缺乏症]
- 钴转运蛋白缺乏症
- 钴转运蛋白II缺乏症
- 钴转运蛋白II缺乏性贫血 [possible translation]
- 钴转运蛋白II缺乏性贫血
- 由于选择遗传性维生素B12吸收不良伴有蛋白尿的贫血
英文词条（11）
- Hereditary vitamin B12 deficiency anaemia
- congenital intrinsic factor deficiency
- defects of cobalamin metabolism
- megaloblastic anaemia due to hereditary vitamin B12 deficiency
- Hereditary megaloblastic anaemia due to transcobalamin deficiency
- Congenital megaloblastic anaemia due to transcobalamin II deficiency
- TCN2 - [transcobalamin II deficiency]
- transcobalamin II deficiency
- transcobalamin II deficiency anaemia
- transcobalamin deficiency
- Anaemia due to selective hereditary vitamin B12 malabsorption with proteinuria
后组配轴 Postcoordination
该条目未定义后组配轴，直接使用上面的编码即可。后组配是在主干编码之后追加侧别、具体解剖部位、严重程度、病因等细节的可选组合方式，不是必填项。