{"Name":"Cor triatriatum dexter","DiseaseID__c":"GARD:0012483","id":12483,"encodedName":"cor-triatriatum-dexter","IsDeleted":false,"Disease_Name_Full__c":"Cor triatriatum dexter","Xref_IDs__c":"274947007; C0344697; HP:0011566; MEDGEN:488867; MONDO:0020429; ORPHA:99098","USA_Estimate__c":null,"No_of_Specialist_Tagsa__c":2,"No_of_ClinGen_records__c":0,"No_of_GeneReviews__c":0,"No_of_HHS_records__c":0,"World_Estimate__c":null,"No_of_HRSA_records__c":0,"Evidence_Based_Score__c":0,"No_of_Disease_Descriptions__c":2,"Disease_Characteristics_Score__c":2,"No_of_Age_at_Onset__c":0,"Description_Source__c":"ORPHA:99098","Disease_Description__c":"A rare, congenital, non-syndromic, heart malformation characterized by the persistence of the embryonic right valve of the sinus venosus which results in a subdivision of right atrium into two chambers. Clinical manifestations depend on the degree of right atrial septation and the size of sinoatrial orifice and vary from asymptomatic to symptoms of tricuspid valve stenosis, atrial fibrillation, cyanosis, syncope, elevated central venous pressure and right heart failure. The anomaly may be isolated or associated with other congenital heart anomalies.","GARD_Name__c":"Cor triatriatum dexter","GARD_Synonym__c":"cor triatriatum dexter (disease); cor triatriatum dextrum; divided right atrium","Curated_Disease_Description_Source__c":"ORPHA:99098","Curated_Disease_Description__c":"A rare, congenital, non-syndromic, heart malformation characterized by the persistence of the embryonic right valve of the sinus venosus which results in a subdivision of right atrium into two chambers. Clinical manifestations depend on the degree of right atrial septation and the size of sinoatrial orifice and vary from asymptomatic to symptoms of tricuspid valve stenosis, atrial fibrillation, cyanosis, syncope, elevated central venous pressure and right heart failure. The anomaly may be isolated or associated with other congenital heart anomalies.","Curated_USA_Estimate_Source__c":null,"Curated_USA_Estimate__c":null,"Age_at_Onset_Snippet_Text__c":null,"SourceID__c":"ORPHA:99098","Deprecated__c":"No","Disease_Concept_Type__c":"Rare Disease Entity","MONDO_ID__c":"MONDO:0020429","ORPHANET_ID__c":"ORPHA:99098","Replaced_By_ID__c":null,"Display_Spanish_Disease_Name__c":"Cor triatriatum dexter","Spanish_Description_Source__c":null,"Spanish_Description__c":null,"Spanish_Disease_Name__c":"cor triatriatum dexter","Spanish_GARD_Synonym__c":"aurícula derecha dividida; cor triatriatum dextrum","Category_Linearization__c":"ORPHA:93890","icd10_id__c":null,"mesh_id__c":null,"omim_id__c":null,"snomed_id__c":null,"umls_id__c":null,"GARD_Disease__c":[{"Curated_Disease_Description__c":"A rare, congenital, non-syndromic, heart malformation characterized by the persistence of the embryonic right valve of the sinus venosus which results in a subdivision of right atrium into two chambers. Clinical manifestations depend on the degree of right atrial septation and the size of sinoatrial orifice and vary from asymptomatic to symptoms of tricuspid valve stenosis, atrial fibrillation, cyanosis, syncope, elevated central venous pressure and right heart failure. The anomaly may be isolated or associated with other congenital heart anomalies.","Curated_Disease_Description_Source__c":"ORPHA:99098","GARD_Synonym__c":"cor triatriatum dexter (disease); cor triatriatum dextrum; divided right atrium","Name":"Cor triatriatum dexter","estimateUsa":""}],"GARD_Disease_Tag__c":[{"Tag_Name__c":"Cardiology","Tag_Category__c":"Specialist"},{"Tag_Name__c":"Congenital Abnormality","Tag_Category__c":"Disease Category","category_description":"Birth defects are structural changes present at birth that can affect almost any part of the body, including how the body looks, works, or both.","curated_tag_name":"Birth defects"},{"Tag_Name__c":"Congenital Heart Disease","Tag_Category__c":"Specialist","curated_tag_name":"Congenital heart disease"}],"External_Identifier_Disease__c":[{"URL__c":"https://browser.ihtsdotools.org/?perspective=full&conceptId1=274947007","Source__c":"C0344697; MONDO:0020429","Xref__c":"274947007"},{"URL__c":"https://www.ncbi.nlm.nih.gov/medgen/?term=488867","Source__c":"C0344697","Xref__c":"MEDGEN:488867"},{"URL__c":"https://www.orpha.net/en/disease/detail/99098","Source__c":"C0344697; MONDO:0020429; ORPHA:99098","Xref__c":"ORPHA:99098"},{"URL__c":"https://uts.nlm.nih.gov/uts/umls/concept/C0344697","Source__c":"C0344697","Xref__c":"C0344697"},{"URL__c":"https://hpo.jax.org/browse/term/HP:0011566","Source__c":"C0344697","Xref__c":"HP:0011566"},{"URL__c":"http://purl.obolibrary.org/obo/MONDO_0020429","Source__c":"GARD:0012483","Xref__c":"MONDO:0020429"}],"tags":{"Specialist":["Cardiology","Congenital Heart Disease"],"Disease Category":["Congenital Abnormality"]},"synonyms":["cor triatriatum dexter (disease)"," cor triatriatum dextrum"," divided right atrium"]}