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Feingold syndrome type 1

Disease definition

Feingold syndrome type 1 (FS1) is a rare inherited malformation syndrome characterized by microcephaly, short stature and numerous digital anomalies.

ORPHA:391641

  • Synonym(s):
    • Brunner-Winter syndrome type 1
    • Digital anomalies with short palpebral fissures and atresia of esophagus or duodenum type 1
    • FGLDS1
    • FS1
    • MMT type 1
    • MODED syndrome type 1
    • Microcephaly-digital anomalies-normal intelligence syndrome type 1
    • Microcephaly-intellectual disability-tracheoesophageal fistula syndrome type 1
    • Microcephaly-oculo-digito-esophageal-duodenal syndrome syndrome type 1
    • ODED syndrome type 1
    • Oculo-digito-esophageal-duodenal syndrome type 1
  • Prevalence: <1 / 1 000 000
  • Inheritance: Autosomal dominant 
  • Age of onset: Infancy, Neonatal
  • ICD-10: Q87.8
  • OMIM: 164280
  • UMLS: -
  • MeSH: -
  • GARD: -
  • MedDRA: -

Detailed information

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Additional information

Further information on this disease

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