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Ontology Browser

Term:
Atrial Septal Defect, Secundum, with Various Cardiac and Noncardiac Defects (DOID:9000778)
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Parent Terms Term With Siblings Child Terms
cleft lip +     
Funnel Chest +     
Hypertelorism +     
Acrootoocular Syndrome 
Ankyloblepharon Filiforme Adnatum 
ankyloblepharon-ectodermal defects-cleft lip/palate syndrome  
atrial fibrillation +   
Atrial Flutter 
atrial heart septal defect 1  
atrial heart septal defect 2  
atrial heart septal defect 3  
atrial heart septal defect 4  
atrial heart septal defect 5  
atrial heart septal defect 6  
atrial heart septal defect 7  
atrial heart septal defect 8  
atrial heart septal defect 9  
Atrial Septal Defect Ostium Primum 
Atrial Septal Defect Sinus Venosus 
Atrial Septal Defect with Atrioventricular Conduction Defects +   
Atrial Septal Defect, Secundum Type 
Atrial Septal Defect, Secundum, with Various Cardiac and Noncardiac Defects 
atrioventricular septal defect +   
Ausems Wittebol-Post Hennekam Syndrome 
autosomal recessive limb-girdle muscular dystrophy type 2X  
Axenfeld-Rieger Anomaly with Cardiac Defects and Sensorineural Hearing Loss 
Bagatelle Cassidy syndrome 
Baraitser Rodeck Garner syndrome 
Barber-Say syndrome  
blepharocheilodontic syndrome +   
Brachycephalofrontonasal Dysplasia  
Bradycardia +   
Brugada syndrome +   
Camptodactyly Syndrome, Guadalajara, Type II 
Camptodactyly Syndrome, Guadalajara, Type III 
Cardiac Arrhythmia, Ankyrin-B-Related  
Cardiac Complexes, Premature +   
Cardiac Conduction Defect, Nonprogressive  
Cardiac Conduction Disease with or without Dilated Cardiomyopathy  
Cardiac Malformation, Cleft Lip-Palate, Microcephaly and Digital Anomalies  
chromosome 6pter-p24 deletion syndrome 
chronic atrial and intestinal dysrhythmia  
Ciuffo Syndrome 
Cleft Lip with or without Cleft Palate, Nonsyndromic, 7 
Cleft Lip with or without Cleft Palate, Nonsyndromic, 8 
Cleft Lip, Congenital Healed 
Commotio Cordis 
Craniosynostosis Mental Retardation Clefting Syndrome 
De Hauwere Leroy Adriaenssens syndrome 
De Hauwere syndrome 
Dursun Syndrome  
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1 
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3  
EEC syndrome +   
Facial Abnormalities, Kyphoscoliosis, and Mental Retardation 
Familial Popliteal Pterygium Syndrome 
Frontonasal Dysplasia 1  
Frontonasal Dysplasia 2  
Frontonasal Dysplasia 3  
Gastrocutaneous Syndrome 
Gillessen-Kaesbach-Nishimura Dysplasia  
Hamamy Syndrome  
Hay Wells Syndrome Recessive Type 
Heart Block +   
Hirschsprung Disease with Polydactyly, Renal Agenesis, and Deafness 
Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate  
Holt-Oram syndrome  
Holzgreve-Wagner-Rehder syndrome 
Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect  
Hyperphosphatasia with Mental Retardation Syndrome 1  
Hypertelorism and Tetralogy of Fallot 
hypertelorism, microtia, facial clefting syndrome 
HYPERTELORISM, PREAURICULAR SINUS, PUNCTAL PITS, AND DEAFNESS 
Hypodontia Oligodontia with Orofacial Cleft 
Hypospadias, Hypertelorism, Upper Lid Coloboma, and Mixed-Type Hearing Loss 
Hypotrichosis, Progressive Patterned Scalp, with Wiry Hair, Onycholysis, and Cleft Lip/Palate 
INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC ARRHYTHMIA  
INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPERTELORISM AND DISTINCTIVE FACIES  
Irons Bhan Syndrome 
Kallmann Syndrome 2 with Cleft Lip or Palate 
Kapur Toriello Syndrome 
Krauss Herman Holmes Syndrome 
Kuster Syndrome 
LANGUAGE DELAY AND ATTENTION DEFICIT-HYPERACTIVITY DISORDER/COGNITIVE IMPAIRMENT WITH OR WITHOUT CARDIAC ARRHYTHMIA  
Larsen syndrome  
long QT syndrome +   
Lutembacher's syndrome 
Lymphedema, Cardiac Septal Defects, And Characteristic Facies 
Marles Greenberg Persaud Syndrome  
Martinez Monasterio Pinheiro Syndrome 
McPherson Clemens Syndrome 
Median Cleft Lip, Corpus Callosum, Lipoma, and Skin Polyps 
Microcephaly, Corpus Callosum Dysgenesis and Cleft Lip-Palate 
Naguib-Richieri-Costa Syndrome 
Oculootofacial Dysplasia +   
Opitz-GBBB syndrome +   
Parasystole 
patent foramen ovale  
Pectus Excavatum, Macrocephaly, Short Stature, Dysplastic Nails 
Peters plus syndrome  
Pilotto Syndrome 
popliteal pterygium syndrome +   
Pre-Excitation Syndromes +   
QT Interval, Variation In 
Radial Ray Deficiency, X-Linked 
rapadilino syndrome  
Rapp-Hodgkin syndrome  
Recurrent Metabolic Encephalomyopathic Crises with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration  
Ritscher-Schinzel syndrome +   
Roberts syndrome  
Rosselli-Gulienetti Syndrome 
Sakoda Complex 
Samson Viljoen Syndrome 
Santos Mateus Leal Syndrome 
Schwartz-Lelek Syndrome  
Seaver Cassidy Syndrome 
Selective Tooth Agenesis with Orofacial Cleft 
short QT syndrome +   
Short Stature, Mental Retardation, Callosal Agenesis, Heminasal Hypoplasia, Microphthalmia, and Atypical Clefting 
Simpson-Golabi-Behmel syndrome type 1  
Sinus Arrhythmia +   
Tachycardia +   
Tel Hashomer Camptodactyly Syndrome 
Thomas Syndrome 
Tibia, Bowing of, with Pseudarthrosis and Pectus Excavatum 
Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations  
uveal coloboma-cleft lip and palate-intellectual disability  
Van der Woude syndrome +   
Van der Woude Syndrome 2  
Ventricular Fibrillation +   
Ventricular Flutter 
Woodhouse-Sakati Syndrome  
Yim Ebbin Syndrome 
Zori Stalker Williams Syndrome 

Synonyms
Primary IDs: MESH:C566351 ;   RDO:0014729

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