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Human Disease and Mouse Model Detail
Human Disease Feingold Syndrome 1; FGLDS1
OMIM ID: 164280
Synonyms Digital Anomalies with Short Palpebral Fissures and Atresia of Esophagus or Duodenum; Feingold Syndrome; Microcephaly and Digital Abnormalities with Normal Intelligence; Microcephaly, Mental Retardation, and Tracheoesophageal Fistula Syndrome; Microcephaly-Oculo-Digito-Esophageal-Duodenal Syndrome; MODED; MMT Syndrome; Oculodigitoesophagoduodenal Syndrome; ODED; ODED Syndrome
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Gene is associated with the disease in this species
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Mycn MYCN*   1:1 Homology

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
07/15/2014
MGI 5.18
The Jackson Laboratory