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Disease Ontology Browser
Feingold syndrome (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
Alt IDs: OMIM:164280, OMIM:614326, ICD10CM:Q87.8, MESH:C537734, ORDO:1305
Definition: An autosomal dominant disease characterized by variable combinations of microcephaly, limb malformations, esophageal and duodenal atresias, and learning disability/mental retardation.

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
06/13/2017
MGI 6.10
The Jackson Laboratory