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congenital disorder of digestive system

AttributesValues
rdf:type
description
  • congenital disorder of digestive system (en)
  • vrozená vada trávicí soustavy (cs)
  • Condição médica (pt)
  • syndrome associant une polypose recto-colique familiale (fr)
  • вроджене захворювання травної системи (uk)
  • wrodzona choroba układu pokarmowego (pl)
  • indrome di natura genetica, caratterizzata dalla presenza di polipi multipli di tipo adenomatoso (it)
exact match
exact match
health specialty
Mondo ID
DiseasesDB
Mondo ID
health specialty
Mondo ID
  • MONDO_0019336
DiseasesDB
  • 5094
rdfs:label
  • Zespół Gardnera (pl)
  • Gardner's syndrome (en)
  • Gardner-Syndrom (de)
  • Gardnerin oireyhtymä (fi)
  • Gardnerův syndrom (cs)
  • Qardner sindromu (az)
  • Síndrome de Gardner (pt)
  • sindrome di Gardner (it)
  • syndrome de Gardner (fr)
  • синдром Ґарднера (uk)
  • متلازمة غاردنر (ar)
  • ガードナー症候群 (ja)
  • 加德納綜合征 (zh-cn)
  • 加德納綜合征 (zh-hans)
  • 加德納綜合徵 (zh-hant)
  • 嘉得氏症 (zh)
  • 가드너 증후군 (ko)
skos:prefLabel
  • Zespół Gardnera (pl)
  • Gardner's syndrome (en)
  • Gardner-Syndrom (de)
  • Gardnerin oireyhtymä (fi)
  • Gardnerův syndrom (cs)
  • Qardner sindromu (az)
  • Síndrome de Gardner (pt)
  • sindrome di Gardner (it)
  • syndrome de Gardner (fr)
  • синдром Ґарднера (uk)
  • متلازمة غاردنر (ar)
  • ガードナー症候群 (ja)
  • 加德納綜合征 (zh-cn)
  • 加德納綜合征 (zh-hans)
  • 加德納綜合徵 (zh-hant)
  • 嘉得氏症 (zh)
  • 가드너 증후군 (ko)
name
  • Zespół Gardnera (pl)
  • Gardner's syndrome (en)
  • Gardner-Syndrom (de)
  • Gardnerin oireyhtymä (fi)
  • Gardnerův syndrom (cs)
  • Qardner sindromu (az)
  • Síndrome de Gardner (pt)
  • sindrome di Gardner (it)
  • syndrome de Gardner (fr)
  • синдром Ґарднера (uk)
  • متلازمة غاردنر (ar)
  • ガードナー症候群 (ja)
  • 加德納綜合征 (zh-cn)
  • 加德納綜合征 (zh-hans)
  • 加德納綜合徵 (zh-hant)
  • 嘉得氏症 (zh)
  • 가드너 증후군 (ko)
Freebase ID
Freebase ID
  • /m/03x42r
image
instance of
image
  • http://commons.wikimedia.org/wiki/Special:FilePath/Gardner1.jpg
instance of
subclass of
subclass of
eMedicine ID
eMedicine ID
  • 1093486
Orphanet ID
ICD-9-CM
genetic association
ICD-10-CM
GARD rare disease ID
OMIM ID
Orphanet ID
  • 79665
ICD-9-CM
  • 759.89
genetic association
ICD-10-CM
  • D12.6
GARD rare disease ID
  • 6482
OMIM ID
  • 175100
named after
named after
Commons category
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