Search Ontology:
Human Disease

Feingold syndrome

Term ID
DOID:0060464
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 )
Relationships
is a type of
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Genes Involved
Zebrafish Models