Feingold syndrome (Q5441566)
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autosomal dominant disease characterized by variable combinations of microcephaly, limb malformations, esophageal and duodenal atresias, and learning disability/mental retardation
- FGLDS
- MODED syndrome
- ODED syndrome
- digital anomalies with short palpebral fissures and atresia of esophagus or duodenum
- microcephaly-digital anomalies-normal intelligence syndrome
- microcephaly-oculo-digito-esophageal-duodenal syndrome
- oculo-digito-esophageal-duodenal syndrome
- MMT
- FS
- Microcephaly-intellectual disability-tracheoesophageal fistula syndrome
- Microcephaly-oculo-digito-esophageal-duodenal syndrome syndrome
- Brunner-Winter syndrome
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Feingold syndrome |
autosomal dominant disease characterized by variable combinations of microcephaly, limb malformations, esophageal and duodenal atresias, and learning disability/mental retardation |
|
Statements
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C74987
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Identifiers
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Sitelinks
Wikipedia(4 entries)
- dewiki Feingold-Syndrom
- enwiki Feingold syndrome
- itwiki Sindrome di Feingold
- plwiki Zespół Feingolda