OBO ID: DOID:0060464
Term Name: Feingold syndrome Search Ontology:
Synonyms:
  • digital anomalies with short palpebral fissures and atresia of esophagus or duodenum
  • FGLDS
  • microcephaly-digital anomalies-normal intelligence syndrome
  • microcephaly-oculo-digito-esophageal-duodenal syndrome
  • MODED syndrome
  • oculo-digito-esophageal-duodenal syndrome
  • ODED syndrome
Definition: A syndrome characterized by variable combinations of microcephaly, limb malformations, esophageal and duodenal atresias, and learning disability/mental retardation. (4)
References:
Ontology: Human Disease   (DOID:0060464)
OTHER Feingold syndrome PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
MYCN Feingold syndrome 1 164280
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None