| 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 |
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Genes and mouse models |
There are currently no human or mouse genes associated with this disease in the MGI database. |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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Citing These Resources Funding Information Warranty Disclaimer & Copyright Notice Send questions and comments to User Support. |
last database update 06/05/2013 MGI 5.13 |
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