Feingold Syndrome 1 (FGLDS1)

Feingold综合征1型(来自ICD-11)

别称:

Feingold Syndrome

Oculodigitoesophagoduodenal Syndrome

Digital Anomalies with Short Palpebral Fissures and Atresia of Esophagus or Duodenum

Oded Syndrome

Microcephaly-Digital Anomalies-Normal Intelligence Syndrome

Microcephaly-Oculo-Digito-Esophageal-Duodenal Syndrome

Oculo-Digito-Esophageal-Duodenal Syndrome

Feingold Syndrome Type 1

Brunner-Winter Syndrome

Moded Syndrome

Mmt Syndrome

Fglds1

Fglds

Microcephaly-Intellectual Disability-Tracheoesophageal Fistula Syndrome

Microcephaly-Oculo-Digito-Esophageal-Duodenal Syndrome Syndrome

Moded

Oded

Mmt

Digital Anomalies with Short Palpebral Fissures and Atresia of Esophagus or Duodenum Type 1

Microcephaly-Intellectual Disability-Tracheoesophageal Fistula Syndrome Type 1

Microcephaly, Mental Retardation, and Tracheoesophageal Fistula Syndrome

Microcephaly-Oculo-Digito-Esophageal-Duodenal Syndrome Syndrome Type 1

Microcephaly-Mesobrachyphalangy-Tracheoesophageal Fistula Syndrome

Microcephaly-Digital Anomalies-Normal Intelligence Syndrome Type 1

Microcephaly Mesobrachyphalangy Tracheoesophageal Fistula Syndrome

Microcephaly and Digital Abnormalities with Normal Intelligence

Microcephaly-Oculo-Digito-Esophageal-Duodenal Syndrome

Oculo-Digito-Esophageal-Duodenal Syndrome Type 1

Oculo-Digito-Esophagoduodental Syndrome

Brunner-Winter Syndrome Type 1

Feingold Syndrome, Type 1

Moded Syndrome Type 1

Oded Syndrome Type 1

Mmt Type 1

Fs1

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基础信息

疾病表征

基因 & 突变

靶点药物

疾病模型

文献报道

Feingold 综合征 1，也被称为 Feingold 综合征，与食管闭锁和肛门闭锁有关。Feingold 综合征 1 的一个重要相关基因是 MYCN (MYCN 原癌基因，BHLH 转录因子)，其相关通路/超通路包括参与 DNA 损伤反应的 miRNA 和在败血症中参与免疫反应的 miRNA。相关组织包括小肠和骨，相关表型包括小头畸形和短指症。

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