SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Hereditary disease  32895009

Autosomal hereditary disorder  1899006

Autosomal dominant hereditary disorder  11164009

Feingold syndrome   702431004

SNOMED CT code


SNOMED code702431004
nameFeingold syndrome
statusactive
date introduced2014-07-31
fully specified name(s)Microcephaly-oculo-digito-esophageal-duodenal syndrome (disorder)
synonyms
  • Feingold syndrome
  • Microcephaly-mesobrachyphalangy-tracheoesophageal fistula syndrome
  • Microcephaly-oculo-digito-esophageal-duodenal syndrome
  • Microcephaly-oculo-digito-oesophageal-duodenal syndrome
  • Oculo-digito-oesophagoduodenal syndrome
  • Oculo-digito-esophagoduodenal syndrome
parentsAutosomal dominant hereditary disorder   11164009
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal dominant hereditary disorder   11164009
              Feingold syndrome   702431004

ancestors
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