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
  • Andersen Tawil syndrome   422348008
  • Atrioventricular septal defect associated with tetralogy of Fallot   448007000
  • 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
  • Carney complex   733491005
  • Carney complex, trismus, pseudocamptodactyly syndrome   766881008
  • 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 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 rhabdomyoma of heart   64862009
  • Criss-cross heart   253269002
  • Ectopia cordis   78250005
  • Eisenmenger's complex   204311009
  • Endocardial cushion defect   15459006
  • 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
  • Hydrocephalus with endocardial fibroelastosis and cataract syndrome   721015008
  • Intellectual disability, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth   412787009
  • Kallman syndrome with heart disease   722027009
  • Kousseff syndrome   726083008
  • Larsen-like syndrome B3GAT3 type   763778003
  • Lethal faciocardiomelic dysplasia   719400000
  • Lung agenesis with heart defect and thumb anomaly syndrome   721976003
  • Malaligned outlet septum   264086008
  • Meacham syndrome   722461004
  • Microcephalus with cardiac defect and lung malsegmentation syndrome   719379001
  • Microcephaly, seizure, intellectual disability, heart disease syndrome   723304001
  • Multiple congenital cardiac defects   94702005
  • 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
  • Primary endocardial fibroelastosis   8239009
  • Short stature with webbed neck and congenital heart disease syndrome   721073008
  • Sonoda syndrome   715987000
  • Thomas syndrome   716740009
  • 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
    Finding by site   118234003
      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 by site   118234003
      Disorder by body site   123946008
        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 by site   118234003
      Disorder by body site   123946008
        Disorder of trunk   128121009
          Disorder of thoracic segment of trunk   609622007
            Congenital anomaly of upper trunk   363037003
              Congenital anomaly of thorax   363035006
                Congenital heart disease   13213009

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