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Human Disease and Mouse Model Detail
Human Disease Feingold Syndrome 1; FGLDS1
OMIM ID: 164280
Human Phenotype Ontology associations
Synonyms Digital Anomalies with Short Palpebral Fissures and Atresia of Esophagus or Duodenum; Feingold Syndrome; 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

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     MYCN* Mycn   HomoloGene and HGNC

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
MGI 6.07
The Jackson Laboratory