Congenital heart disease   13213009

SNOMED CT code


SNOMED code13213009
nameCongenital heart disease
statusactive
date introduced2002-01-31
fully specified name(s)Congenital heart disease (disorder)
synonyms
  • Congenital heart disease
  • Congenital anomaly of heart
  • CHD - Congenital heart disease
attributes - group1
Associated morphologyMorphologically abnormal structure   49755003
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Finding siteHeart structure   80891009
parents
  • Structural disorder of heart   128599005
  • Congenital anomaly of cardiovascular structure of trunk   363028003
  • Congenital anomaly of thorax   363035006
children
  • 3C syndrome   718556007
  • [X]Congenital malformations of cardiac chambers and connections   205889004  removed: 2009-01-31
  • [X]Other congenital malformations of cardiac chambers and connections   205872007  removed: 2009-01-31
  • [X]Other congenital malformations of cardiac septa   205873002  removed: 2009-01-31
  • [X]Other specified congenital malformations of the heart   205878006  removed: 2009-01-31
  • Acyanotic congenital heart disease   78485007
  • Atrioventricular septal defect associated with tetralogy of Fallot   448007000
  • Autosomal dominant intellectual disability, craniofacial anomalies, cardiac defects syndrome   1255319004
  • Beemer Ertbruggen syndrome   717859007
  • Bifid apex of heart   444851003
  • Bosley Salih Alorainy syndrome   720567008
  • Brain malformation, congenital heart disease, postaxial polydactyly syndrome   717943008
  • Bulbus cordis and cardiac septal closure anomalies   268174004
  • Cardiac anomaly and heterotaxy syndrome   720605009
  • Cardiocranial syndrome Pfeiffer type   720606005
  • Cataract, congenital heart disease, neural tube defect syndrome   726704006
  • Cleft lip and cleft palate with intestinal malrotation and cardiopathy syndrome   719456001
  • Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome   720639008
  • Complex congenital heart defect   63191000119107
  • Congenital abnormality of cardiac connection   253272009
  • Congenital abnormality of cardiac vein   447938004
  • Congenital abnormality of relationship of cardiac component   253267000
  • Congenital absence of heart structure   413905004
  • Congenital anomaly of cardiac chamber   15964981000119104
  • Congenital anomaly of coronary artery   28574005
  • Congenital anomaly of heart valve   70320004
  • Congenital anomaly of myocardium   204394002
  • Congenital cardiomegaly   48121000
  • Congenital endocardial fibroelastosis   1141882007
  • Congenital epicardial cyst   204398004
  • Congenital heart anomaly NOS   204413006  removed: 2010-01-31
  • Congenital heart disease in pregnancy   237227006
  • Congenital heart disease, septal and bulbar anomalies   253264007
  • Congenital hypoplasia of heart   93262004
  • Congenital malposition of cardiac apex   51789008
  • Congenital malposition of heart   10818008
  • Congenital vertebral, cardiac, renal anomalies syndrome   1260142000
  • Criss-cross heart   253269002
  • Cyanotic congenital heart disease   12770006
  • Ectopia cordis   78250005
  • Eisenmenger's complex   204311009
  • Facial dysmorphism, conductive hearing loss, heart defect syndrome   763279007
  • Faciocardiorenal syndrome   723333000
  • False tendon - heart   264467005
  • Fatal congenital nonlysosomal heart glycogenosis   459062008
  • Genitopalatocardiac syndrome   773749003
  • Hadziselimovic syndrome   719395001
  • Heart defect and limb shortening syndrome   721009008
  • Heart defect, tongue hamartoma, polysyndactyly syndrome   783738002
  • Heart-hand syndrome type 2   721010003
  • Heart-hand syndrome type 3   721013001
  • Hemicardia   204399007
  • Holt-Oram syndrome   19092004
  • Intellectual disability, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth   412787009
  • Jervell and Lange-Nielsen syndrome   373905003
  • Kallman syndrome with heart disease   722027009
  • Kousseff syndrome   726083008
  • Larsen-like syndrome B3GAT3 type   763778003
  • Lethal brain and heart developmental defects syndrome   1229876001
  • Lethal faciocardiomelic dysplasia   719400000
  • Lung agenesis with heart defect and thumb anomaly syndrome   721976003
  • Meacham syndrome   722461004
  • Microcephalus with cardiac defect and lung malsegmentation syndrome   719379001
  • Microcephaly, seizure, intellectual disability, heart disease syndrome   723304001
  • Mucopolysaccharidosis-like plus disease   1187113001
  • Multiple congenital cardiac defects   94702005
  • Neurodevelopmental disorder, craniofacial dysmorphism, cardiac defect, skeletal anomalies syndrome   1222710008
  • Obesity, colitis, hypothyroidism, cardiac hypertrophy, developmental delay syndrome   722051004
  • Oro-facial digital syndrome type 11   718681002
  • Oro-facial digital syndrome type 12   763834000
  • Oro-facial digital syndrome type 13   763835004
  • Other congenital heart anomalies   204338002  removed: 2010-01-31
  • Other specified heart anomalies   204367001  removed: 2010-01-31
  • Pancreatic hypoplasia, diabetes mellitus, congenital heart disease syndrome   722206009
  • Partial defect of atrioventricular canal   718216009
  • Pericarditis secondary to Mulibrey nanism   31080005
  • Polysyndactyly and cardiac malformation syndrome   724066002
  • Short stature with webbed neck and congenital heart disease syndrome   721073008
  • Short stature, developmental delay, congenital heart defect syndrome   1237512003
  • Sonoda syndrome   715987000
  • Thomas syndrome   716740009
  • TMEM94-associated congenital heart defect, facial dysmorphism, developmental delay syndrome   1222708006
  • TRAF7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome   1208998007
  • Vascular ring with malrotation and dextroversion of heart and hypoplasia of right lung and left arterial duct   448305002
  • Verloove Vanhorick Brubakk syndrome   764697003
  • Williams syndrome   63247009
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Cardiovascular finding   106063007
      Cardiac finding   301095005
        Heart disease   56265001
          Structural disorder of heart   128599005
            Congenital heart disease   13213009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of trunk structure   302292003
      Disorder of trunk   128121009
        Congenital anomaly of trunk   78626001
          Congenital anomaly of cardiovascular structure of trunk   363028003
            Congenital heart disease   13213009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of trunk structure   302292003
      Finding of upper trunk   609623002
        Finding of region of thorax   298705000
          Disorder of thorax   118946009
            Congenital anomaly of thorax   363035006
              Congenital heart disease   13213009

ancestors
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