ICD-11 编码查询_国际疾病分类第 11 版中文版_在线疾病编码检索工具
5A00.03

暂时性先天性甲状腺功能减退

Transient congenital hypothyroidism

上级条目
5A00.0 先天性甲状腺功能减退症
层级
6 级

定义

一过性先天性甲状腺功能减退是指一过性甲状腺功能减退,促甲状腺激素(TSH)轻度升高,甲状腺素(FT4)水平较低,可迅速自发恢复正常,或经过几个月甲状腺素治疗后恢复正常。这种疾病是由多种原因引起,包括缺碘或接触含碘化合物、阻断母体抗体的經胎盤途徑和激素生成障碍。

Transient congenital hypothyroidism is defined as transient thyroid dysfunction with mildly elevated thyroid-stimulating hormone (TSH) and low thyroxine (FT4) levels which return to normal either very promptly and spontaneously, or after several months of thyroxine therapy. The disorder is due to a variety of causes including iodine deficiency or exposure to iodine-containing compounds, transplacental passage of blocking maternal antibodies, and dyshormonogenesis.

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英文词条(1)

索引词 可用于检索该条目的同义词与别名

  • 暂时性先天性甲状腺功能减退
  • 双氧化酶2突变的单等位或双等位基因突变引起的短暂的先天性甲状腺功能减退症
  • DUOX2突变的单等位或双等位突变的杂合突变引起的短暂的先天性甲状腺功能减退症
  • 由于母体摄入抗甲状腺药物引起的短暂的先天性甲状腺功能减退症
  • 由于母体碘缺乏或过量引起的短暂的先天性甲状腺功能减退症
  • 胎儿碘综合征
  • 新生儿碘缺乏或过量引起的短暂的先天性甲状腺功能减退
  • 新生儿碘暴露引起的短暂的先天性甲状腺功能减退
  • 母体TSH受体阻断抗体的经胎盘途经引起的短暂的先天性甲状腺功能减退症
  • THOX2的杂合突变引起的短暂的先天性甲状腺功能减退症
英文词条(10)
  • Transient congenital hypothyroidism
  • Transient congenital hypothyroidism due to monoallelic or biallelic mutations of dual oxidase 2 mutation
  • Transient congenital hypothyroidism due to heterozygous mutations of monoallelic or biallelic mutations of DUOX2 mutation
  • Transient congenital hypothyroidism due to maternal intake of antithyroid drugs
  • Transient congenital hypothyroidism due to maternal iodine deficiency or excess
  • Fetal iodine syndrome
  • Transient congenital hypothyroidism due to neonatal iodine deficiency or excess
  • Transient congenital hypothyroidism due to neonatal iodine exposure
  • Transient congenital hypothyroidism due to transplacental passage of maternal TSH receptor blocking antibodies
  • Transient congenital hypothyroidism due to heterozygous mutations of THOX2

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。