Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Ontology Browser

Term:
atrial heart septal defect 3 (DOID:0110108)
Annotations: Rat: (1) Mouse: (1) Human: (2) Chinchilla: (0) Bonobo: (1) Dog: (0) Squirrel: (0) Pig: (0)
Parent Terms Term With Siblings Child Terms
Adrenocortical Hypofunction, Chronic Primary Congenital 
adrenocorticotropic hormone deficiency  
advanced sleep phase syndrome 3  
age related macular degeneration 8  
Alagille syndrome  
Alpha-2-Deficient Collagen Disease 
apparent mineralocorticoid excess syndrome  
Aquaporin 1 Deficiency 
aspartylglucosaminuria  
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 23  
cataract 25 
cataract 26 multiple types 
cataract 27  
cataract 28 
Cenani-Lenz syndactyly syndrome  
CHARGE syndrome  
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 +   
desquamative interstitial pneumonia  
Dursun Syndrome  
Dwarfism +   
Familial Cirrhosis +   
Familial Dysalbuminemic Hyperthyroxinemia  
Familial Hemophagocytic Lymphohistiocytoses +   
familial hypertrophic cardiomyopathy +   
Familial Lipochrome Histiocytosis 
Familial Mixed Cryoglobulinemia  
Familial Temporal Epilepsy +   
frontotemporal dementia and/or amyotrophic lateral sclerosis-3  
frontotemporal dementia and/or amyotrophic lateral sclerosis-4  
Genetic Skin Diseases +   
hereditary angioedema +   
Hereditary Bilateral Parotidomegaly 
Hereditary Epistaxis 
Hereditary Eye Diseases +   
hereditary lymphedema +   
Hereditary Neoplastic Syndromes +   
Holt-Oram syndrome  
hypogonadotropic hypogonadism 5 with or without anosmia +   
inherited metabolic disorder +   
Irons Bhan Syndrome 
Isolated Prolactin Deficiency 
Kallmann syndrome +   
Laminopathies  
Lennox-Gastaut syndrome  
Lutembacher's syndrome 
Lymphatic Malformation 7  
Lymphedema, Cardiac Septal Defects, and Characteristic Facies 
Marfan syndrome +   
monogenic disease +   
Nervous System Heredodegenerative Disorders +   
Nonimmune Chronic Idiopathic Neutropenia, Adult  
Oculootofacial Dysplasia +   
osteochondrodysplasia +   
patent foramen ovale  
polygenic disease +   
primary hypertrophic osteoarthropathy +   
progressive familial intrahepatic cholestasis +   
pulmonary alveolar microlithiasis  
Radial Ray Deficiency, X-Linked 
rapadilino syndrome  
Ritscher-Schinzel syndrome +   
Sacral Agenesis with Vertebral Anomalies  
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 "DO"

paths to the root