Allowable subheadings

Aarskog Syndrome Disease MeSH Browser

Al Gazali Aziz Salem syndrome Disease MeSH Browser

Amastia, Bilateral, With Ureteral Triplication And Dysmorphism Disease MeSH Browser

Aplasia Cutis Congenita, Congenital Heart Defect, And Frontonasal Cysts Disease MeSH Browser

Arterial Occlusive Disease, Progressive, with Hypertension, Heart Defects, Bone Fragility, and Brachysyndactyly Disease MeSH Browser

Baetz-Greenwalt syndrome Disease MeSH Browser

Beemer Ertbruggen syndrome Disease MeSH Browser

Bixler Christian Gorlin syndrome Disease MeSH Browser

Blepharophimosis syndrome Ohdo type Disease MeSH Browser

Bonneau Syndrome Disease MeSH Browser

Burn-Mckeown syndrome Disease MeSH Browser

Cardiac Malformation, Cleft Lip-Palate, Microcephaly and Digital Anomalies Disease MeSH Browser

Cardiac Valvular Defect, Developmental Disease MeSH Browser

Cardiac valvular dysplasia, X-linked Disease MeSH Browser

Cardioauditory syndrome of Sanchez Cascos Disease MeSH Browser

Cardiocranial syndrome Disease MeSH Browser

Cardiofaciocutaneous syndrome Disease MeSH Browser

Chromosome 1q21.1 Duplication Syndrome Disease MeSH Browser

Chromosome 6pter-P24 Deletion Syndrome Disease MeSH Browser

Cleft Palate, Cardiac Defect, Genital Anomalies, and Ectrodactyly Disease MeSH Browser

Congenital Heart Defects, X-Linked Disease MeSH Browser

Conotruncal cardiac defects Disease MeSH Browser

Corpus Callosum, Agenesis of, with Facial Anomalies and Robin Sequence Disease MeSH Browser

Cranioacrofacial Syndrome Disease MeSH Browser

Craniofacial Abnormalities, Cataracts, Congenital Heart Disease, Sacral Neural Tube Defects, and Growth and Developmental Retardation Disease MeSH Browser

Craniofaciofrontodigital Syndrome Disease MeSH Browser

Deafness, Congenital Heart Defects, and Posterior Embryotoxon Disease MeSH Browser

Distichiasis with Congenital Anomalies of the Heart and Peripheral Vasculature Disease MeSH Browser

Ectrodactyly cardiopathy dysmorphism Disease MeSH Browser

Ectrodactyly of Lower Limbs, Congenital Heart Defect, and Micrognathia Disease MeSH Browser

Ellis Yale Winter syndrome Disease MeSH Browser

Emanuel syndrome Disease MeSH Browser

Faciocardiomelic Dysplasia, Lethal Disease MeSH Browser

Faciocardiomelic Syndrome Disease MeSH Browser

Faciocardiorenal syndrome Disease MeSH Browser

Familial anomalous origin of right pulmonary artery Disease MeSH Browser

Fragile Site 16p12 Disease MeSH Browser

Frontoocular Syndrome Disease MeSH Browser

Gay Feinmesser Cohen syndrome Disease MeSH Browser

Genito palato cardiac syndrome Disease MeSH Browser

Growth and Developmental Retardation, Ocular Ptosis, Cardiac Defect, and Anal Atresia Disease MeSH Browser

Heart defects limb shortening Disease MeSH Browser

Heart-hand syndrome, Slovenian type Disease MeSH Browser

Heart-hand syndrome, Spanish type Disease MeSH Browser

Hecht Scott syndrome Disease MeSH Browser

Hirschsprung Disease with Heart Defects, Laryngeal Anomalies, and Preaxial Polydactyly Disease MeSH Browser

Hirschsprung Disease, Cardiac Defects, and Autonomic Dysfunction Disease MeSH Browser

Hittner Hirsch Kreh syndrome Disease MeSH Browser

Ho Kaufman Mcalister syndrome Disease MeSH Browser

Holt-Oram syndrome Disease MeSH Browser

Holzgreve Wagner Rehder syndrome Disease MeSH Browser

Hydrolethalus syndrome Disease MeSH Browser

Kasznica Carlson Coppedge syndrome Disease MeSH Browser

Kleefstra Syndrome Disease MeSH Browser

Lowry Maclean syndrome Disease MeSH Browser

Malpuech facial clefting syndrome Disease MeSH Browser

McDonough syndrome Disease MeSH Browser

McKusick Kaufman syndrome Disease MeSH Browser

McPherson Clemens syndrome Disease MeSH Browser

Mehta Lewis Patton syndrome Disease MeSH Browser

Mexican Cardiomelic Dysplasia Disease MeSH Browser

Microcephaly seizures mental retardation heart disorders Disease MeSH Browser

Microcephaly, Congenital Heart Disease, Unilateral Renal Agenesis, and Hyposegmented Lungs Disease MeSH Browser

Noncompaction of Left Ventricular Myocardium with Congenital Heart Defects Disease MeSH Browser

Orstavik Lindemann Solberg syndrome Disease MeSH Browser

Pancreatic Hypoplasia, Congenital, with Diabetes Mellitus and Congenital Heart Disease Disease MeSH Browser

Pilotto syndrome Disease MeSH Browser

Powell Chandra Saal syndrome Disease MeSH Browser

Pseudodiastrophic dysplasia Disease MeSH Browser

Pulmonary Atresia with Intact Ventricular Septum Disease MeSH Browser

Right ventricle hypoplasia Disease MeSH Browser

Rommen Mueller Sybert syndrome Disease MeSH Browser

Saal Bulas syndrome Disease MeSH Browser

Sacral meningocele conotruncal heart defects Disease MeSH Browser

Scimitar Anomaly, Multiple Cardiac Malformations, and Craniofacial and Central Nervous System Abnormalities Disease MeSH Browser

Short QT Syndrome 1 Disease MeSH Browser

Short QT Syndrome 2 Disease MeSH Browser

Short QT Syndrome 3 Disease MeSH Browser

Simpson-Golabi-Behmel syndrome Disease MeSH Browser

Sonoda syndrome Disease MeSH Browser

Steinfeld Syndrome Disease MeSH Browser

Stratton-Parker Syndrome Disease MeSH Browser

Subaortic Stenosis, Membranous Disease MeSH Browser

TARP syndrome Disease MeSH Browser

Tabatznik syndrome Disease MeSH Browser

Tamari Goodman syndrome Disease MeSH Browser

Ter Haar syndrome Disease MeSH Browser

Thomas syndrome Disease MeSH Browser

Uhl anomaly Disease MeSH Browser

VACTERL association Disease MeSH Browser

VATER association Disease MeSH Browser

Vater Association With Hydrocephalus Disease MeSH Browser

Vater-Like Defects with Pulmonary Hypertension, Laryngeal Webs, and Growth Deficiency Disease MeSH Browser

Ventricular extrasystoles perodactyly Robin sequence Disease MeSH Browser

Verloove-Vanhorick Brubakk syndrome Disease MeSH Browser

Young Simpson syndrome Disease MeSH Browser

Zunich neuroectodermal syndrome Disease MeSH Browser

aorto-atrial tunnel Disease MeSH Browser