Congenital anomaly of digestive system 69518005 SNOMED CT code SNOMED code 69518005 name Congenital anomaly of digestive system status active date introduced 2002-01-31 fully specified name(s) Congenital anomaly of digestive system (disorder) synonyms Congenital anomaly of digestive system Congenital deformity of digestive system Congenital malformation of the digestive system attributes - group1 Pathological process Pathological developmental process 308490002 Associated morphology Morphologically abnormal structure 49755003 Occurrence Congenital 255399007 Finding site Digestive structure 86762007 parents children [X]Other congenital malformations of the digestive system 205905009 removed: 2009-01-31 [X]Other specified congenital malformations of digestive system 205923001 removed: 2009-01-31 Congenital absence of digestive system NOS 204813003 removed: 2010-01-31 Congenital anomaly of digestive organ 128332003 Congenital anomaly of digestive tract 95470009 Congenital arteriovenous malformation of gastrointestinal tract 95471008 Congenital mesenteric cyst 253802003 Congenital mesocolic hernia 86595004 Digestive system anomalies NOS 204820005 removed: 2010-01-31 Gastrointestinal tract congenital anomalies NOS 287084005 removed: 2010-01-31 GIT congenital anomaly 275261001 removed: 2004-07-31 Hereditary splenic hypoplasia 302961007 Infantile botulism 230680004 removed: 2005-01-31 Other congenital digestive system anomaly 204684000 removed: 2010-01-31 Other congenital upper alimentary tract anomalies 204624003 removed: 2010-01-31 Other GIT congenital anomaly 268325007 removed: 2010-01-31 Persistent dorsal mesentery 123662000 Primary Sjögren's syndrome with multisystem involvement 239914005 removed: 2020-01-31 Secondary Sjögren's syndrome with multisystem involvement 239917003 removed: 2020-01-31 Universal mesentery 52159006 hierarchies a selection of possible paths
SNOMED CT Concept 138875005 404684003 64572001 5294002 276654001 69518005 138875005 404684003 118234003 386617003 53619000 69518005 ancestors sorted most to least specific
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