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Ontology Browser

Term:
Distichiasis with Congenital Anomalies of the Heart and Peripheral Vasculature (DOID:9007928)
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Parent Terms Term With Siblings Child Terms
22q11 Deletion Syndrome +   
3MC syndrome 3  
Aarskog syndrome +   
acrocardiofacial syndrome 
Agenesis of Corpus Callosum with Facial Anomalies and Robin Sequence 
Al Gazali Aziz Salem Syndrome 
Alagille syndrome +   
Aortic Coarctation +   
aortic valve disease 1  
aortic valve disease 3  
Aortico-Ventricular Tunnel 
Aplasia Cutis Congenita, Congenital Heart Defect, and Frontonasal Cysts 
arrhythmogenic right ventricular cardiomyopathy +   
arterial tortuosity syndrome  
Arterio-Arterial Fistula +  
arteriovenous malformation +   
Baetz-Greenwalt Syndrome 
Barth syndrome +   
Beaulieu-Boycott-Innes Syndrome  
Beemer Ertbruggen Syndrome 
Bilateral Amastia with Ureteral Triplication and Dysmorphism 
Bonneau Syndrome 
Cardiac Valvular Dysplasia +   
Cardiac-Urogenital Syndrome  
Cardioacrofacial Dysplasia +   
Cardioauditory Syndrome of Sanchez Cascos 
Cardiocranial Syndrome 
cardiofaciocutaneous syndrome +   
Cardiofacioneurodevelopmental Syndrome  
Central Nervous System Vascular Malformations +   
CHIME syndrome  
chromosome 1q21.1 duplication syndrome  
chromosome 6pter-p24 deletion syndrome 
CLEFT LIP AND PALATE-CRANIOFACIAL DYSMORPHISM-CONGENITAL HEART DEFECT-HEARING LOSS SYNDROME  
cleft palate, cardiac defects, and intellectual disabillity  
CLOVES 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  
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 
familial multiple nevi flammei  
Frank-Ter Haar syndrome  
Frontoocular Syndrome 
Gay Feinmesser Cohen Syndrome 
Genito Palato Cardiac Syndrome 
Grange Syndrome  
Growth and Developmental Retardation, Ocular Ptosis, Cardiac Defect, and Anal Atresia 
Heart Defects Limb Shortening 
heart septal defect +   
Heart-Hand Syndrome, Slovenian Type  
Hecht Scott Syndrome 
Hemophilia A with Vascular Abnormality 
hereditary hemorrhagic telangiectasia +   
Hirschsprung Disease with Heart Defects, Laryngeal Anomalies, and Preaxial Polydactyly 
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  
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  
Lethal Faciocardiomelic Dysplasia 
Levocardia 
long QT syndrome +   
Lowry Maclean syndrome 
Marfan syndrome +   
May-Thurner Syndrome 
McDonough Syndrome 
McKusick-Kaufman syndrome  
McPherson Clemens Syndrome 
Meacham Winn Culler Syndrome  
Mehta Lewis Patton Syndrome 
Membranous Subaortic Stenosis 
Meningioangiomatosis 
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 
Microcephaly-Capillary Malformation Syndrome  
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  
patent ductus arteriosus +   
Patent Ductus Venosus  
Pilotto Syndrome 
Powell Chandra Saal Syndrome 
Prepapillary Vascular Loops 
Primary Intraosseous Vascular Malformation  
Pseudodiastrophic Dysplasia 
Pulmonary Atresia +   
Pulmonary Atresia with Intact Ventricular Septum  
retinal arterial tortuosity  
Right Ventricle Hypoplasia  
Rommen Mueller Sybert Syndrome 
Saal Bulas Syndrome 
Sacral Meningocele Conotruncal Heart Defects 
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  
Single Umbilical Artery 
Sonoda Syndrome 
Splenoportal Vascular Anomalies 
Steinfeld Syndrome 
Stratton-Parker Syndrome 
Structural Heart Defects and Renal Anomalies Syndrome  
Tabatznik Syndrome 
Tamari Goodman Syndrome 
TARP syndrome  
Testicular Anomalies with or without Congenital Heart Disease  
Thomas Syndrome 
tricuspid atresia +   
Trilogy of Fallot 
Turner syndrome +   
Uhl Anomaly 
VACTERL association +   
Vascular Fistula +   
Vater-Like Defects with Pulmonary Hypertension, Laryngeal Webs, and Growth Deficiency 
Ventricular Extrasystoles Perodactyly Robin Sequence 
Verloove-Vanhorick Brubakk Syndrome 
visceral heterotaxy +   
Wolff-Parkinson-White syndrome  
X-linked cardiac valvular dysplasia  

Synonyms
Primary IDs: MESH:C565092
Alternate IDs: MIM:126320

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