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C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities: Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] > Congenital Abnormalities [MESH:D000013] > Cardiovascular Abnormalities [MESH:D018376] > Heart Defects, Congenital [MESH:D006330]
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The current query selects 2611 items in 131 groups, which could be too many to show at once. If you are sure you want to see them all, you can proceed to see the entire category, 'or select a more specific subcategory of "Heart Defects, Congenital [MESH:D006330]" below.

Subcategories in C16. Congenital, Hereditary, and Neonatal Diseases and AbnormalitiesCongenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] > Congenital Abnormalities [MESH:D000013] > Cardiovascular Abnormalities [MESH:D018376] > Heart Defects, Congenital [MESH:D006330]:
(jump to A - B - C - D - E - F - G - H - I - J - K - L - M - N - O - P - R - S - T - U - V - W - Y - Z - other)
- A -
Aarskog Syndrome [MESH:C535331] (18)
Al Gazali Aziz Salem syndrome [MESH:C535613] (1)
Alagille Syndrome [MESH:D016738] (105)
Amastia, Bilateral, With Ureteral Triplication And Dysmorphism [MESH:C566295] (1)
Aortic Coarctation [MESH:D001017] (6)
Aortic Valve Disease [MESH:C563178] (1)
Aplasia Cutis Congenita, Congenital Heart Defect, And Frontonasal Cysts [MESH:C566997] (1)
Arrhythmogenic Right Ventricular Dysplasia [MESH:D019571] (241)
Arterial Occlusive Disease, Progressive, with Hypertension, Heart Defects, Bone Fragility, and Brachysyndactyly [MESH:C566529] (1)
 
- B -
Baetz-Greenwalt syndrome [MESH:C537795] (1)
Barth Syndrome [MESH:D056889] (13)
Beemer Ertbruggen syndrome [MESH:C537668] (1)
Bixler Christian Gorlin syndrome [MESH:C537632] (1)
Blepharophimosis syndrome Ohdo type [MESH:C536232] (1)
Bonneau Syndrome [MESH:C564875] (1)
Burn-Mckeown syndrome [MESH:C537411] (1)
 
- C -
Cardiac Malformation, Cleft Lip-Palate, Microcephaly and Digital Anomalies [MESH:C563414] (1)
Cardiac Valvular Defect, Developmental [MESH:C565882] (1)
Cardiac valvular dysplasia, X-linked [MESH:C535576] (36)
Cardioauditory syndrome of Sanchez Cascos [MESH:C535577] (1)
Cardiocranial syndrome [MESH:C535578] (1)
Cardiofaciocutaneous syndrome [MESH:C535579] (407)
Chromosome 1q21.1 Duplication Syndrome [MESH:C567290] (1)
Chromosome 6pter-P24 Deletion Syndrome [MESH:C567239] (1)
Cleft Palate, Cardiac Defect, Genital Anomalies, and Ectrodactyly [MESH:C563936] (1)
Congenital Heart Defects, X-Linked [MESH:C567444] (1)
Conotruncal cardiac defects [MESH:C535464] (2)
Cor Triatriatum [MESH:D003310] (1)
Coronary Vessel Anomalies [MESH:D003330] (317)
Corpus Callosum, Agenesis of, with Facial Anomalies and Robin Sequence [MESH:C563127] (1)
Cranioacrofacial Syndrome [MESH:C565147] (1)
Craniofacial Abnormalities, Cataracts, Congenital Heart Disease, Sacral Neural Tube Defects, and Growth and Developmental Retardation [MESH:C564271] (1)
Craniofaciofrontodigital Syndrome [MESH:C567298] (1)
Crisscross Heart [MESH:D003420] (1)
 
- D -
Deafness, Congenital Heart Defects, and Posterior Embryotoxon [MESH:C566604] (1)
Dextrocardia [MESH:D003914] (61)
Distichiasis with Congenital Anomalies of the Heart and Peripheral Vasculature [MESH:C565092] (1)
Ductus Arteriosus, Patent [MESH:D004374] (325)
 
- E -
Ebstein Anomaly [MESH:D004437] (6)
Ectopia Cordis [MESH:D054083] (1)
Ectrodactyly cardiopathy dysmorphism [MESH:C536187] (1)
Ectrodactyly of Lower Limbs, Congenital Heart Defect, and Micrognathia [MESH:C563344] (1)
Eisenmenger Complex [MESH:D004541] (1)
Ellis Yale Winter syndrome [MESH:C536205] (1)
Emanuel syndrome [MESH:C535733] (1)
 
- F -
Faciocardiomelic Dysplasia, Lethal [MESH:C565578] (1)
Faciocardiomelic Syndrome [MESH:C567176] (1)
Faciocardiorenal syndrome [MESH:C536388] (1)
Familial anomalous origin of right pulmonary artery [MESH:C535681] (1)
Fragile Site 16p12 [MESH:C565001] (1)
Frontoocular Syndrome [MESH:C565340] (1)
 
- G -
Gay Feinmesser Cohen syndrome [MESH:C537676] (1)
Genito palato cardiac syndrome [MESH:C537683] (1)
Growth and Developmental Retardation, Ocular Ptosis, Cardiac Defect, and Anal Atresia [MESH:C565755] (1)
 
- H -
Heart Septal Defects [MESH:D006343] (385)
Heart defects limb shortening [MESH:C535850] (1)
Heart-hand syndrome, Slovenian type [MESH:C535852] (77)
Heart-hand syndrome, Spanish type [MESH:C535853] (1)
Hecht Scott syndrome [MESH:C535856] (1)
Heterotaxy Syndrome [MESH:D059446] (84)
Hirschsprung Disease with Heart Defects, Laryngeal Anomalies, and Preaxial Polydactyly [MESH:C565817] (1)
Hirschsprung Disease, Cardiac Defects, and Autonomic Dysfunction [MESH:C563939] (1)
Hittner Hirsch Kreh syndrome [MESH:C538323] (1)
Ho Kaufman Mcalister syndrome [MESH:C538325] (1)
Holt-Oram syndrome [MESH:C535326] (11)
Holzgreve Wagner Rehder syndrome [MESH:C535327] (1)
Hydrolethalus syndrome [MESH:C536079] (9)
Hypoplastic Left Heart Syndrome [MESH:D018636] (194)
 
- I -
Isolated Noncompaction of the Ventricular Myocardium [MESH:D056830] (4)
 
- J -
Jarcho-Levin syndrome [MESH:C537565] (1)
 
 - K -
Kasznica Carlson Coppedge syndrome [MESH:C537011] (1)
Kleefstra Syndrome [MESH:C563043] (25)
 
- L -
LEOPARD Syndrome [MESH:D044542] (299)
Levocardia [MESH:D007979] (1)
Long QT Syndrome [MESH:D008133] (693)
Lowry Maclean syndrome [MESH:C537037] (1)
 
- M -
Malpuech facial clefting syndrome [MESH:C535704] (45)
Marcus Gunn phenomenon [MESH:C535908] (2)
Marfan Syndrome [MESH:D008382] (646)
McDonough syndrome [MESH:C538158] (1)
McKusick Kaufman syndrome [MESH:C538159] (17)
McPherson Clemens syndrome [MESH:C538160] (1)
Meacham Syndrome [MESH:C563821] (1)
Mehta Lewis Patton syndrome [MESH:C536147] (1)
Mexican Cardiomelic Dysplasia [MESH:C563087] (1)
Microcephaly seizures mental retardation heart disorders [MESH:C537544] (1)
Microcephaly, Congenital Heart Disease, Unilateral Renal Agenesis, and Hyposegmented Lungs [MESH:C563341] (1)
 
- N -
Noncompaction of Left Ventricular Myocardium with Congenital Heart Defects [MESH:C564690] (1)
Noonan Syndrome [MESH:D009634] (506)
 
- O -
Orstavik Lindemann Solberg syndrome [MESH:C537137] (1)
 
- P -
Pancreatic Hypoplasia, Congenital, with Diabetes Mellitus and Congenital Heart Disease [MESH:C564011] (1)
Pilotto syndrome [MESH:C537400] (1)
Powell Chandra Saal syndrome [MESH:C538357] (1)
Pseudodiastrophic dysplasia [MESH:C535826] (1)
Pulmonary Atresia with Intact Ventricular Septum [MESH:C562832] (1)
 
- R -
Right ventricle hypoplasia [MESH:C535682] (1)
Rommen Mueller Sybert syndrome [MESH:C535871] (1)
 
- S -
Saal Bulas syndrome [MESH:C537193] (1)
Sacral meningocele conotruncal heart defects [MESH:C537223] (1)
Scimitar Anomaly, Multiple Cardiac Malformations, and Craniofacial and Central Nervous System Abnormalities [MESH:C564262] (1)
Short QT Syndrome 1 [MESH:C566506] (189)
Short QT Syndrome 2 [MESH:C566505] (45)
Short QT Syndrome 3 [MESH:C566504] (39)
Simpson-Golabi-Behmel syndrome [MESH:C537340] (45)
Sonoda syndrome [MESH:C536680] (1)
Steinfeld Syndrome [MESH:C566655] (1)
Stratton-Parker Syndrome [MESH:C566105] (1)
Subaortic Stenosis, Membranous [MESH:C564793] (1)
 
- T -
TARP syndrome [MESH:C536942] (18)
Tabatznik syndrome [MESH:C536784] (1)
Tamari Goodman syndrome [MESH:C536896] (1)
Ter Haar syndrome [MESH:C537274] (13)
Tetralogy of Fallot [MESH:D013771] (121)
Thomas syndrome [MESH:C536514] (1)
Transposition of Great Vessels [MESH:D014188] (60)
Tricuspid Atresia [MESH:D018785] (6)
Trilogy of Fallot [MESH:D014286] (1)
Turner Syndrome [MESH:D014424] (131)
 
- U -
Uhl anomaly [MESH:C536932] (1)
 
- V -
VACTERL association [MESH:C536495] (2)
VACTERL association with hydrocephaly, X-linked [MESH:C536520] (16)
VACTERL hydrocephaly [MESH:C536521] (151)
VATER association [MESH:C536534] (46)
Vater Association With Hydrocephalus [MESH:C564752] (1)
Vater-Like Defects with Pulmonary Hypertension, Laryngeal Webs, and Growth Deficiency [MESH:C564244] (1)
Ventricular extrasystoles perodactyly Robin sequence [MESH:C536537] (1)
Verloove-Vanhorick Brubakk syndrome [MESH:C536541] (1)
 
- W -
Wolff-Parkinson-White Syndrome [MESH:D014927] (40)
 
- Y -
Young Simpson syndrome [MESH:C536717] (1)
 
- Z -
Zunich neuroectodermal syndrome [MESH:C536729] (1)
 
- other -
22q11 Deletion Syndrome [MESH:D058165] (237)