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Ontology Browser

Term:
atrial heart septal defect 3 (DOID:0110108)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (0) Bonobo: (1) Dog: (1) Squirrel: (0) Pig: (0)
Parent Terms Term With Siblings Child Terms
Adrenocortical Hypofunction, Chronic Primary Congenital 
adrenocorticotropic hormone deficiency  
advanced sleep phase syndrome 1  
advanced sleep phase syndrome 2  
advanced sleep phase syndrome 3  
age related macular degeneration 8  
Alagille syndrome  
Alpha-2-Deficient Collagen Disease 
Alzheimer's disease 18  
AQUAPORIN 1 DEFICIENCY  
ataxia telangiectasia +   
ataxic cerebral palsy 
atrial heart septal defect 1  
atrial heart septal defect 2  
atrial heart septal defect 3  
An atrial heart septal defect type 3 that has material basis in heterozygous mutation in the myosin heavy chain-6 gene (MYH6) on chromosome 14q12. (DO)
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 +   
autoimmune lymphoproliferative syndrome +   
Axenfeld-Rieger Anomaly with Cardiac Defects and Sensorineural Hearing Loss 
brachydactyly type A1B 
brachydactyly type A1C  
brachydactyly type A1D  
brachydactyly type B1  
brachydactyly type B2  
brachydactyly type E1  
brachydactyly type E2  
CADASIL +   
CAKUT2  
cataract 1 multiple types  
cataract 10 multiple types  
cataract 11 multiple types +   
cataract 12 multiple types  
cataract 13 with adult i phenotype  
cataract 14 multiple types  
cataract 15 multiple types  
cataract 16 multiple types  
cataract 18  
cataract 2 multiple types  
cataract 20 multiple types  
cataract 21 multiple types  
cataract 23  
cataract 24 
cataract 25 
cataract 26 multiple types 
cataract 27  
cataract 28 
cataract 29 
cataract 3 multiple types  
cataract 30  
cataract 31 multiple types  
cataract 33  
cataract 36  
cataract 37 
cataract 38  
cataract 41  
cataract 42  
cataract 43  
cataract 44  
cataract 45  
cataract 46 juvenile-onset  
Cataract 48  
cataract 5 multiple types  
cataract 7  
cataract 8 multiple types 
cataract 9 multiple types  
Cenani-Lenz syndactyly syndrome  
CHARGE syndrome  
cherubism +   
chromosomal disease +   
Ciuffo Syndrome 
complement factor I deficiency  
complex cortical dysplasia with other brain malformations 1  
complex cortical dysplasia with other brain malformations 2  
complex cortical dysplasia with other brain malformations 3  
complex cortical dysplasia with other brain malformations 4  
complex cortical dysplasia with other brain malformations 5  
complex cortical dysplasia with other brain malformations 6  
complex cortical dysplasia with other brain malformations 7  
congenital diarrhea +   
congenital hemolytic anemia +   
Congenital Hepatic Fibrosis  
congenital hypoplastic anemia +   
congenital muscular dystrophy +   
congenital myasthenic syndrome +   
Congenital Pain Insensitivity +   
corneal opacification and other ocular anomalies +   
desquamative interstitial pneumonia  
Dursun Syndrome  
Dwarfism +   
dystonia 5  
Familial Cirrhosis +   
Familial Dysalbuminemic Hyperthyroxinemia  
Familial Hemophagocytic Lymphohistiocytoses +   
familial hypertrophic cardiomyopathy +   
Familial Lipochrome Histiocytosis 
Familial Mixed Cryoglobulinemia  
Familial Temporal Epilepsy +   
FTDALS3  
FTDALS4  
Genetic Skin Diseases +   
hereditary angioedema +   
Hereditary Epistaxis 
Hereditary Eye Diseases +   
hereditary lymphedema +   
Hereditary Neoplastic Syndromes +   
Holt-Oram syndrome  
Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect  
hyperekplexia 1  
hyperimmunoglobulin syndrome +   
hypogonadotropic hypogonadism 5 with or without anosmia +   
IMMUNODEFICIENCY 31B  
Immunodeficiency 38, with Basal Ganglia Calcification  
inherited blood coagulation disease +   
inherited metabolic disorder +   
Irons Bhan Syndrome 
Isolated Prolactin Deficiency 
Kallmann syndrome +   
Kartagener syndrome  
Laminopathies  
Lennox-Gastaut syndrome  
Lutembacher's syndrome 
Lymphedema, Cardiac Septal Defects, And Characteristic Facies 
Marfan syndrome +   
MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY  
monogenic disease +   
Nervous System Heredodegenerative Disorders +   
Nonimmune Chronic Idiopathic Neutropenia, Adult  
Oculootofacial Dysplasia +   
osteochondrodysplasia +   
Parotidomegaly, Hereditary Bilateral 
patent foramen ovale  
platelet-type bleeding disorder 10  
polycystic kidney disease +   
polygenic disease +   
primary hypertrophic osteoarthropathy +   
progressive familial intrahepatic cholestasis +   
pulmonary alveolar microlithiasis  
Radial Ray Deficiency, X-Linked 
rapadilino syndrome  
RASopathies  
Rh deficiency syndrome  
Ritscher-Schinzel syndrome +   
Sacral Agenesis with Vertebral Anomalies  
sclerosteosis 2  
Tel Hashomer Camptodactyly Syndrome 
yellow nail syndrome +  

Synonyms
Exact Synonyms: ASD3 ;   atrial septal defect 3
Primary IDs: MESH:C563540 ;   RDO:0012768
Alternate IDs: OMIM:614089 ;   RDO:9000137
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/15735645

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