GB90.44
肾小管性酸中毒
Renal tubular acidosis
- 上级条目
- GB90.4 肾小管功能疾患
- 层级
- 5 级
定义
以肾脏不能排泄酸或碳酸氢盐不能进入尿液为特征的疾病，导致血液过酸的情况。特征为高氯性酸中毒（低阴离子间隙代谢性酸中毒）。有多种形式和多种原因。
Conditions characterised by failure of the kidney to excrete acids, or to lose bicarbonate into the urine, which causes the blood to become too acidic. Characteristically hyperchloremic acidosis (low anion gap metabolic acidosis). Has several forms and many causes.
肾脏无法将酸性物质排入尿液，导致血液酸性过高。血液长期酸性导致生长迟缓、肾结石、骨病、慢性肾病，甚至可能导致肾功能完全衰竭。
跨章引用 同一概念在其他章节另有编码
索引词 可用于检索该条目的同义词与别名
- 肾小管性酸中毒
- 莱特伍德-奥尔布赖特综合征
- 莱特伍德综合征
- 特发性婴儿高钙血症-轻度
- RTA[肾小管性酸中毒] [possible translation]
- 肾性酸中毒 [possible translation]
- 肾小管性酸中毒 [possible translation]
- 肾性酸中毒 [possible translation]
- 肾高氯性酸中毒 [possible translation]
- 肾小管性酸中毒 [possible translation]
- 肾高氯性酸中毒
- 肾性酸中毒
- RTA[肾小管性酸中毒]
- 肾小管性酸中毒
- 肾性酸中毒
- 肾小管性酸中毒
- 肾小管酸中毒-聋
- 常染色体隐性遗传远端肾小管酸中毒伴聋
- 获得性肾小管酸中毒
- 家族性或遗传性疾患引起的肾小管酸中毒
- I型肾小管酸中毒
- 远端肾小管酸中毒
- 分类于他处的家族性或遗传性疾病引起的远端肾小管酸中毒
- 分类于他处的家族性或遗传性疾病引起的远端肾小管酸中毒1型
- 散发性先天性肾小管酸中毒1型
- 常染色体显性遗传肾小管酸中毒1型
- 常染色体隐性遗传肾小管酸中毒1型
- 分类于他处的系统性疾患引起的肾小管酸中毒1型
- 获得性远端肾小管酸中毒
- 获得性远端肾小管酸中毒1型
- II型肾小管酸中毒
- 近端肾小管酸中毒
- 家族性或遗传性疾病引起的近端肾小管酸中毒
- 家族性和遗传性疾病引起的近端肾小管酸中毒2型
- 家族性单纯型近端肾小管酸中毒
- 家族性单纯型近端肾小管酸中毒2型
- 近端肾小管酸中毒伴眼部异常和智力缺陷
- 获得性近端肾小管酸中毒，原因分类于他处
- 获得性近端肾小管酸中毒2型，原因分类于他处
- III型肾小管酸中毒
- 混合性近端-远端肾小管酸中毒
- 碳酸酐酶II缺乏
英文词条（36）
- Renal tubular acidosis
- Lightwood syndrome
- Lightwood-Albright syndrome
- RTA - [renal tubular acidosis]
- idiopathic infantile hypercalcemia - mild form
- kidney acidosis
- kidney tubular acidosis
- renal acidosis
- renal hyperchloremic acidosis
- renal tubule acidosis
- Renal tubular acidosis - deafness
- Autosomal recessive distal renal tubular acidosis with deafness
- Acquired renal tubular acidosis
- Renal tubular acidosis due to familial or genetic disorders
- Type I renal tubular acidosis
- Distal renal tubular acidosis
- Distal renal tubular acidosis due to familial or genetic disease classified elsewhere
- Distal Type 1 renal tubular acidosis due to familial and genetic disease classified elsewhere
- Sporadic congenital renal tubular acidosis type 1
- Autosomal dominant renal tubular acidosis type 1
- Autosomal recessive renal tubular acidosis type 1
- Renal tubular acidosis type 1 due to systemic disorders elsewhere classified
- Acquired distal renal tubular acidosis
- Acquired distal Type 1 renal tubular acidosis
- Type II renal tubular acidosis
- Proximal renal tubular acidosis
- Proximal renal tubular acidosis due to familial or genetic disease
- Proximal Type 2 renal tubular acidosis due to familial and genetic disease
- Familial pure proximal renal tubular acidosis
- Familial pure proximal Type 2 renal tubular acidosis
- Proximal renal tubular acidosis with ocular abnormalities and intellectual deficit
- Acquired proximal renal tubular acidosis with causes elsewhere classified
- Acquired proximal Type 2 renal tubular acidosis with causes elsewhere classified
- Type III renal tubular acidosis
- Mixed proximal-distal renal tubular acidosis
- Carbonic anhydrase II deficiency
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