Feingold syndrome

Summary
Synonym
  • FGLDS
  • MODED syndrome
  • ODED syndrome
  • digital anomalies with short palpebral fissures and atresia of esophagus or duodenum
  • microcephaly-digital anomalies-normal intelligence syndrome
  • microcephaly-oculo-digito-esophageal-duodenal syndrome
  • oculo-digito-esophageal-duodenal syndrome
Definition
A syndrome characterized by variable combinations of microcephaly, limb malformations, esophageal and duodenal atresias, and learning disability/mental retardation.
Super Class
autosomal dominant disease syndrome
Disease Ontology
DOID:0060464
Mondo Disease Ontology
MeSH
ORDO
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
4613 MYCN MYCN proto-oncogene, bHLH transcription factor
Displaying 1 entry
Gene ID Gene Symbol Description Source
18109 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024