罕见病知识库 RareSeen

Complex neurodevelopmental disorder with unspecific dysmorphic features/congenital anomalies without intellectual disability or autism spectrum disorder

ORPHA:730421疾病暂无中文名

定义 英文原文(暂无中文)

A rare neurodevelopmental disorder characterized by the combination of at least two neurodevelopmental disorders, including specific learning disorder (e.g., impairment in reading, written expression, or mathematics), motor disorder (e.g. developmental coordination disorder, stereotypic movement disorder, tic disorder), communication disorder (e.g., developmental language disorder, speech sound disorder, childhood-onset fluency disorder, social/pragmatic communication disorder), attention deficit/hyperactivity disorder (ADD/ADHD) and other specified or unspecified neurodevelopmental disorders as defined in DSM-5 or ICD-11. Patients don't reach the criteria of an autism spectrum disorder diagnosis, do not have intellectual disability but can present with unspecific dysmorphic features and/or congenital anomalies.

外部标识与链接

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本页数据来源

  • 疾病定义、同义词、基因、表型、流行病学:Orphanet(CC BY 4.0)
  • 中文病名:Orphanet 中文包,冻结于 2020-06-01;本条目在该版本中无中文名
  • 表型中文标签:HPO 简体中文翻译(CHPO 上游成果)