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Ontology Browser

Term:
Hirschsprung Disease, Cardiac Defects, and Autonomic Dysfunction (DOID:9001782)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
22q11 Deletion Syndrome +   
3MC syndrome 3  
Aarskog syndrome +   
Adie syndrome 
Agenesis of Corpus Callosum with Facial Anomalies and Robin Sequence 
Al Gazali Aziz Salem Syndrome 
Al Gazali Hirschsprung Syndrome 
Alagille syndrome  
Aortic Coarctation +   
aortic valve disease 1  
Aortic Valve Disease 3  
Aplasia Cutis Congenita, Congenital Heart Defect, and Frontonasal Cysts 
arrhythmogenic right ventricular cardiomyopathy +   
Au-Kline Syndrome  
Autonomic Dysreflexia 
autonomic neuropathy +   
Baetz-Greenwalt syndrome 
Barth syndrome +   
Beaulieu-Boycott-Innes Syndrome  
Beemer Ertbruggen Syndrome 
Bilateral Amastia with Ureteral Triplication and Dysmorphism 
Bonneau Syndrome 
Bresheck/Bresek Syndrome 
Cardiac-Urogenital Syndrome  
Cardioauditory Syndrome of Sanchez Cascos 
Cardiocranial Syndrome 
cardiofaciocutaneous syndrome +   
Cartilage Hair Hypoplasia Like Syndrome 
cartilage-hair hypoplasia  
CHIME syndrome  
chromosome 1q21.1 duplication syndrome 
chromosome 6pter-p24 deletion syndrome 
Cleft Palate, Cardiac Defect, Genital Anomalies, and Ectrodactyly 
cleft palate, cardiac defects, and intellectual disabillity  
complex regional pain syndrome +  
congenital central hypoventilation syndrome  
CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA  
CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME  
Congenital Heart Defects, Dysmorphic Facial Features, and Intellectual Developmental Disorder  
congenital heart defects, hamartomas of tongue, and polysyndactyly  
Congenital Heart Defects, Multiple Types +   
Congenital Heart Defects, X-Linked +   
Conotruncal Cardiac Defects  
Cor Triatriatum 
Coronary Vessel Anomalies +   
Cranioacrofacial Syndrome 
Craniofacial Abnormalities, Cataracts, Congenital Heart Disease, Sacral Neural Tube Defects, and Growth and Developmental Retardation 
Craniofaciofrontodigital Syndrome 
Crisscross Heart 
Deafness, Congenital Heart Defects, and Posterior Embryotoxon  
developmental cardiac valvular defect  
dextro-looped transposition of the great arteries +   
dextrocardia +   
Distichiasis with Congenital Anomalies of the Heart and Peripheral Vasculature 
Ebstein anomaly  
Ectopia Cordis 
Ectrodactyly Cardiopathy Dysmorphism 
Ectrodactyly of Lower Limbs, Congenital Heart Defect, and Micrognathia 
Eisenmenger Complex  
Ellis Yale Winter Syndrome 
Emanuel Syndrome 
Faciocardiomelic Syndrome 
Faciocardiorenal Syndrome 
Familial Anomalous Origin of Right Pulmonary Artery 
Fragile Site 16p12 
Frank-Ter Haar syndrome  
Frey syndrome 
Frontoocular Syndrome 
Gay Feinmesser Cohen Syndrome 
Genito Palato Cardiac Syndrome 
Goldberg-Shprintzen syndrome  
Grange Syndrome  
Growth and Developmental Retardation, Ocular Ptosis, Cardiac Defect, and Anal Atresia 
Harlequin Syndrome 
Heart Defects Limb Shortening 
heart septal defect +   
Heart-Hand Syndrome, Slovenian Type  
Heart-Hand Syndrome, Spanish Type 
Hecht Scott Syndrome 
Hirschsprung Disease 1  
Hirschsprung Disease Ganglioneuroblastoma  
Hirschsprung Disease Polydactyly Heart Disease 
Hirschsprung Disease Type 3 
Hirschsprung Disease Type d Brachydactyly 
Hirschsprung Disease with Heart Defects, Laryngeal Anomalies, and Preaxial Polydactyly 
Hirschsprung Disease with Polydactyly, Renal Agenesis, and Deafness 
Hirschsprung Disease with Ulnar Polydactyly, Polysyndactyly of Big Toes, and Ventricular Septal Defect 
Hirschsprung Disease, Cardiac Defects, and Autonomic Dysfunction  
Hittner Hirsch Kreh Syndrome  
Ho Kaufman Mcalister Syndrome 
Holt-Oram syndrome  
Holzgreve-Wagner-Rehder syndrome 
hydrolethalus syndrome +   
hypertelorism, microtia, facial clefting syndrome 
hypoplastic left heart syndrome +   
hypoplastic right heart syndrome  
idiopathic peripheral autonomic neuropathy 
Intellectual Developmental Disorder with Cardiac Defects and Dysmorphic Facies  
Isolated Noncompaction of the Ventricular Myocardium +   
jaw-winking syndrome 
Kasznica Carlson Coppedge Syndrome 
Kleefstra syndrome +   
Larsen-like syndrome B3GAT3 type  
Laurence Prosser Rocker Syndrome 
Lethal Faciocardiomelic Dysplasia 
Levocardia 
long QT syndrome +   
Lowry Maclean syndrome 
Marfan syndrome +   
McDonough Syndrome 
McKusick-Kaufman syndrome  
McPherson Clemens Syndrome 
Meacham Winn Culler Syndrome  
Mehta Lewis Patton Syndrome 
Mental Retardation and Distinctive Facial Features with or without Cardiac Defects  
Mexican Cardiomelic Dysplasia 
Microcephaly Seizures Mental Retardation Heart Disorders 
Microcephaly, Congenital Heart Disease, Unilateral Renal Agenesis, and Hyposegmented Lungs 
Motor Neuropathy Peripheral with Dysautonomia 
Mowat-Wilson syndrome  
Neurodevelopmental Disorder with Central and Peripheral Motor Dysfunction  
Neurodevelopmental Disorder with or without Anomalies of the Brain, Eye, or Heart  
Noncompaction of Left Ventricular Myocardium with Congenital Heart Defects 
Noonan syndrome +   
Noonan syndrome with multiple lentigines +   
Ohdo syndrome +   
pancreatic hypoplasia-diabetes-congenital heart disease syndrome  
paroxysmal extreme pain disorder  
patent ductus arteriosus +   
PCWH syndrome  
Pilotto Syndrome 
Plexosarcoma 
Powell Chandra Saal Syndrome 
Primary Dysautonomias +   
Pseudodiastrophic Dysplasia 
Pulmonary Atresia with Intact Ventricular Septum  
Right Ventricle Hypoplasia  
Rommen Mueller Sybert Syndrome 
Saal Bulas Syndrome 
Sacral Meningocele Conotruncal Heart Defects 
Santos Mateus Leal Syndrome 
scimitar syndrome +   
Short QT Syndrome 1  
Short QT Syndrome 2  
Short QT Syndrome 3  
Short Stature, Developmental Delay, and Congenital Heart Defects  
Simpson-Golabi-Behmel syndrome type 1  
Sonoda Syndrome 
Steinfeld Syndrome 
Stratton-Parker Syndrome 
Structural Heart Defects and Renal Anomalies Syndrome  
Subaortic Stenosis, Membranous 
Tabatznik Syndrome 
Tamari Goodman Syndrome 
TARP syndrome  
Testicular Anomalies with or without Congenital Heart Disease  
Thomas Syndrome 
Total Intestinal Aganglionosis  
tricuspid atresia +   
Trilogy of Fallot 
Turner syndrome +   
Uhl Anomaly 
VACTERL association +   
Vater-Like Defects with Pulmonary Hypertension, Laryngeal Webs, and Growth Deficiency 
Ventricular Extrasystoles Perodactyly Robin Sequence 
Verloove-Vanhorick Brubakk Syndrome 
visceral heterotaxy +   
Waardenburg Syndrome Type 4 +   
Wolff-Parkinson-White syndrome  
X-linked cardiac valvular dysplasia  

Synonyms
Exact Synonyms: HCAD
Primary IDs: MESH:C563939 ;   RDO:0013061
Alternate IDs: OMIM:613870

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.