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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

In OMIM:
OMIM:164280 - FEINGOLD SYNDROME 1; FGLDS1
OMIM:614326 - FEINGOLD SYNDROME 2; FGLDS2

In Mondo Disease Ontology:
MONDO:0015267 - Feingold syndrome

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : mycn

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): autosomal dominant disease (is_a), syndrome (is_a)