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Summary Literature (0)
DOID:0060464 - Feingold syndrome

Disease Ontology Definition:A syndrome characterized by variable combinations of microcephaly, limb malformations, esophageal and duodenal atresias, and learning disability/mental retardation.

Synonyms: 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,

Xenbase Genes : mycn

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0015267 - Feingold syndrome

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), syndrome (is_a)