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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: 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
Xenbase Genes
:
mycn
| MONDO:0015267 - Feingold syndrome |
Other Model Organisms: Alliance, 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)