heart defects, congenital

Preferred Label : heart defects, congenital;

MeSH definition : Developmental abnormalities involving structures of the heart. These defects are present at birth but may be discovered later in life.;

MeSH synonym : defects, congenital heart; congenital heart defect; abnormality, heart; congenital heart defects; defect, congenital heart; heart abnormalities; heart defect, congenital; heart abnormality; heart, malformation of; Malformation Of Heart; Malformation Of Hearts; Congenital Heart Disease; Congenital Heart Diseases; Disease, Congenital Heart; Heart Disease, Congenital;

CISMeF synonym : abnormalities, heart;

MeSH annotation : general only; do not use as coordinate for specific term /abnorm; cyanotic defects probably go here but do not also index under CYANOSIS unless especially discussed;

Wikipedia link : https://en.wikipedia.org/wiki/Congenital heart defect;

Details

Origin ID

D006330;

UMLS CUI

C0018798;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Carboplatin/Cisplatin/Cyclophosphamide Regimen [NCIt concept]
- Cardiac Stem Cell [NCIt concept]
- Chronic cor pulmonale (disorder) [SNOMED CT concept]
- Congenital heart disease [ACR pathology]
- Congenital malformation of the right heart [HPO term]
- History of Congenital Heart Disease [NCIt concept]
- Other bulbus cordis anomalies and anomalies of cardiac septal closure [ICD-9 code]
- Other congenital anomalies of heart [ICD-9 code]
- Other congenital malformations of heart [ICD-10 category (who)]
- Papilloma of choroid plexus [OMIM Phenotype]
- Structural developmental anomaly of heart or great vessels [Bloc CIM-11]
- Unspecified defect of septal closure [ICD-9 code]
- With congenital heart disease [ACR pathology]
- With congenital heart disease [ACR pathology]
- With congenital heart disease [ACR pathology]
- congenital anomaly cardiovascular [ICPC-2 Rubric]
- congenital heart disease [DO Concept]
- obsolete Malformation of the heart and great vessels [HPO term]
Currated CISMeF NLP mapping
- Congenital Heart Disease [NCIt concept]
- Congenital heart disease [PASCAL descriptor]
- Congenital heart disease (disorder) [SNOMED CT concept]
- Congenital malformation of heart, unspecified [ICD-10 Sub-category]
- Congenital malformation of heart, unspecified [ICD-10 Sub-category (who)]
- Disease heart congenital (NOS) [MedDRA LLT]
- HEART MALFORMATION [WHO-ART High Level Term]
- Heart Malformation [NCIt concept]
- Heart disease congenital [MedDRA Preferred Term]
- Heart malformation [MedDRA LLT]
- Heart, malformation of [OMIM Phenotype]
- Heart, malformation of [OMIM Phenotype]
- Malformation heart (NOS) [MedDRA LLT]
- Rare congenital non-syndromic heart malformation [ORDO Disease]
- Unspecified congenital anomaly of heart [ICD-9 code]
- congenital heart defects [MedlinePlus Topic]
- congenital heart disease, nos [SNOMED Notion]
- congenital heart malformation [Disease (Nov.)]
- heart disease congenital [TUV Concept]
- heart disease congenital [TUV Term]
- heart malformation [BNCI symptom]
DO Cross reference
- congenital heart disease [DO Concept]
False automatic mappings
- Abnormal heart morphology [HPO term]
HPO term
- Abnormal heart morphology [HPO term]
Manual BTNT mappings - CISMeF
- Atrioventricular discordance [ORDO Disease]
- Atrioventricular valve anomaly [ORDO Disease]
- Cardiac diverticulum [ORDO Disease]
- Congenital pulmonary veins anomaly [ORDO Disease]
- Heart position anomaly [ORDO Disease]
- Rare atrial defect and interatrial communication [ORDO Disease]
- Rare syndrome with cardiac malformations [ORDO Disease]
- Transposition of the great arteries and conotruncal cardiac anomaly [ORDO Disease]
- Univentricular cardiopathy [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Rare developmental defect during embryogenesis [ORDO Disease]
- Rare surgical cardiac disease [ORDO Disease]
MeSH Descriptor(s) used for indexing
- heart [MeSH Descriptor]
- myocardium [MeSH Descriptor]
MedlinePlus topic(s)
- congenital heart defects [MedlinePlus Topic]
Record concept(s)
- heart defects, congenital [MeSH concept]
Related MeSH Supplementary Concept(s)
- Aarskog syndrome [MeSH Supplementary Concept]
- Baetz-Greenwalt syndrome [MeSH Supplementary Concept]
- Burn-Mckeown syndrome [MeSH Supplementary Concept]
- Holt-Oram syndrome [MeSH Supplementary Concept]
- Jarcho-Levin syndrome [MeSH Supplementary Concept]
- McDonough syndrome [MeSH Supplementary Concept]
- McKusick kaufman syndrome [MeSH Supplementary Concept]
- McPherson clemens syndrome [MeSH Supplementary Concept]
- Simpson-Golabi-Behmel syndrome [MeSH Supplementary Concept]
- Stratton-Parker syndrome [MeSH Supplementary Concept]
- TARP syndrome [MeSH Supplementary Concept]
- VACTERL association [MeSH Supplementary Concept]
- VATER association [MeSH Supplementary Concept]
- Vater-Like defects with pulmonary hypertension, laryngeal webs, and growth deficiency [MeSH Supplementary Concept]
- Verloove-Vanhorick brubakk syndrome [MeSH Supplementary Concept]
- al gazali aziz salem syndrome [MeSH Supplementary Concept]
- amastia, bilateral, with ureteral triplication and dysmorphism [MeSH Supplementary Concept]
- aorto-atrial tunnel [MeSH Supplementary Concept]
- aplasia cutis congenita, congenital heart defect, and frontonasal cysts [MeSH Supplementary Concept]
- arterial occlusive disease, progressive, with hypertension, heart defects, bone fragility, and brachysyndactyly [MeSH Supplementary Concept]
- beemer ertbruggen syndrome [MeSH Supplementary Concept]
- bixler christian gorlin syndrome [MeSH Supplementary Concept]
- blepharophimosis syndrome ohdo type [MeSH Supplementary Concept]
- bonneau syndrome [MeSH Supplementary Concept]
- cardiac malformation, cleft Lip-Palate, microcephaly and digital anomalies [MeSH Supplementary Concept]
- cardiac valvular defect, developmental [MeSH Supplementary Concept]
- cardiac valvular dysplasia, X-linked [MeSH Supplementary Concept]
- cardioauditory syndrome of sanchez cascos [MeSH Supplementary Concept]
- cardiocranial syndrome [MeSH Supplementary Concept]
- cardiofaciocutaneous syndrome [MeSH Supplementary Concept]
- chromosome 1q21.1 duplication syndrome [MeSH Supplementary Concept]
- chromosome 6pter-P24 deletion syndrome [MeSH Supplementary Concept]
- cleft palate, cardiac defect, genital anomalies, and ectrodactyly [MeSH Supplementary Concept]
- congenital heart defects, X-Linked [MeSH Supplementary Concept]
- conotruncal cardiac defects [MeSH Supplementary Concept]
- corpus callosum, agenesis of, with facial anomalies and robin sequence [MeSH Supplementary Concept]
- cranioacrofacial syndrome [MeSH Supplementary Concept]
- craniofacial abnormalities, cataracts, congenital heart disease, sacral neural tube defects, and growth and developmental retardation [MeSH Supplementary Concept]
- craniofaciofrontodigital syndrome [MeSH Supplementary Concept]
- deafness, congenital heart defects, and posterior embryotoxon [MeSH Supplementary Concept]
- distichiasis with congenital anomalies of the heart and peripheral vasculature [MeSH Supplementary Concept]
- ectrodactyly cardiopathy dysmorphism [MeSH Supplementary Concept]
- ectrodactyly of lower limbs, congenital heart defect, and micrognathia [MeSH Supplementary Concept]
- ellis yale winter syndrome [MeSH Supplementary Concept]
- emanuel syndrome [MeSH Supplementary Concept]
- faciocardiomelic dysplasia, lethal [MeSH Supplementary Concept]
- faciocardiomelic syndrome [MeSH Supplementary Concept]
- faciocardiorenal syndrome [MeSH Supplementary Concept]
- familial anomalous origin of right pulmonary artery [MeSH Supplementary Concept]
- fragile site 16p12 [MeSH Supplementary Concept]
- frontoocular syndrome [MeSH Supplementary Concept]
- gay feinmesser cohen syndrome [MeSH Supplementary Concept]
- genito palato cardiac syndrome [MeSH Supplementary Concept]
- growth and developmental retardation, ocular ptosis, cardiac defect, and anal atresia [MeSH Supplementary Concept]
- heart defects limb shortening [MeSH Supplementary Concept]
- heart-hand syndrome, slovenian type [MeSH Supplementary Concept]
- heart-hand syndrome, spanish type [MeSH Supplementary Concept]
- hecht scott syndrome [MeSH Supplementary Concept]
- hirschsprung disease with heart defects, laryngeal anomalies, and preaxial polydactyly [MeSH Supplementary Concept]
- hirschsprung disease, cardiac defects, and autonomic dysfunction [MeSH Supplementary Concept]
- hittner hirsch kreh syndrome [MeSH Supplementary Concept]
- ho kaufman mcalister syndrome [MeSH Supplementary Concept]
- holzgreve wagner rehder syndrome [MeSH Supplementary Concept]
- hydrolethalus syndrome [MeSH Supplementary Concept]
- kasznica carlson coppedge syndrome [MeSH Supplementary Concept]
- kleefstra syndrome [MeSH Supplementary Concept]
- lowry maclean syndrome [MeSH Supplementary Concept]
- malpuech facial clefting syndrome [MeSH Supplementary Concept]
- marcus gunn phenomenon [MeSH Supplementary Concept]
- mehta lewis patton syndrome [MeSH Supplementary Concept]
- mexican cardiomelic dysplasia [MeSH Supplementary Concept]
- microcephaly seizures mental retardation heart disorders [MeSH Supplementary Concept]
- microcephaly, congenital heart disease, unilateral renal agenesis, and hyposegmented lungs [MeSH Supplementary Concept]
- noncompaction of left ventricular myocardium with congenital heart defects [MeSH Supplementary Concept]
- orstavik lindemann solberg syndrome [MeSH Supplementary Concept]
- pancreatic hypoplasia, congenital, with diabetes mellitus and congenital heart disease [MeSH Supplementary Concept]
- pilotto syndrome [MeSH Supplementary Concept]
- powell chandra saal syndrome [MeSH Supplementary Concept]
- pseudodiastrophic dysplasia [MeSH Supplementary Concept]
- pulmonary atresia with intact ventricular septum [MeSH Supplementary Concept]
- right ventricle hypoplasia [MeSH Supplementary Concept]
- rommen mueller sybert syndrome [MeSH Supplementary Concept]
- saal bulas syndrome [MeSH Supplementary Concept]
- sacral meningocele conotruncal heart defects [MeSH Supplementary Concept]
- scimitar anomaly, multiple cardiac malformations, and craniofacial and central nervous system abnormalities [MeSH Supplementary Concept]
- short QT syndrome 1 [MeSH Supplementary Concept]
- short QT syndrome 2 [MeSH Supplementary Concept]
- short QT syndrome 3 [MeSH Supplementary Concept]
- sonoda syndrome [MeSH Supplementary Concept]
- steinfeld syndrome [MeSH Supplementary Concept]
- subaortic stenosis, membranous [MeSH Supplementary Concept]
- tabatznik syndrome [MeSH Supplementary Concept]
- tamari goodman syndrome [MeSH Supplementary Concept]
- ter haar syndrome [MeSH Supplementary Concept]
- thomas syndrome [MeSH Supplementary Concept]
- uhl anomaly [MeSH Supplementary Concept]
- vater association with hydrocephalus [MeSH Supplementary Concept]
- ventricular extrasystoles perodactyly robin sequence [MeSH Supplementary Concept]
- young simpson syndrome [MeSH Supplementary Concept]
- zunich neuroectodermal syndrome [MeSH Supplementary Concept]
See also
- cardiovascular abnormalities [MeSH Descriptor]
See also (suggested by CISMeF)
- heart diseases [MeSH Descriptor]
- myocardium [MeSH Descriptor]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Abnormal heart morphology [HPO term]
- Anomaly heart [MedDRA LLT]
- Congenital malformation of heart, unspecified [ICD-10 Sub-category]
- Congenital malformation of heart, unspecified [ICD-10 Sub-category (who)]
- HEART MALFORMATION [WHO-ART High Level Term]
- Heart Malformation [NCIt concept]
- Heart malformation [MedDRA LLT]
- Heart, malformation of [OMIM Phenotype]
- Heart, malformation of [OMIM Phenotype]
- Malformation heart (NOS) [MedDRA LLT]
- Rare congenital non-syndromic heart malformation [ORDO Disease]
- Unspecified congenital anomaly of heart [ICD-9 code]
- Unspecified congenital anomaly of heart [MedDRA LLT]
- congenital heart defects [MedlinePlus Topic]
- congenital heart disease [DO Concept]
- heart malformation [BNCI symptom]

Keyword's position in hierarchy(ies) :

Main resources

You can consult :

recommendations
documents concerning education
documents for patients