{"context":{"query":">>hpo>>orphanet","source_dataset":"hpo","target_dataset":"orphanet"},"stats":{"queried":1,"total":25,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|disorder_type|gene_count|phenotype_count","mappings":[{"input":"HP:0005110","source":"HP:0005110|Atrial fibrillation","targets":["137675|Histiocytoid cardiomyopathy|Disease|1|44","1478|Interatrial communication|Morphological anomaly|0|19","1677|Familial idiopathic dilatation of the right atrium|Morphological anomaly|0|24","1880|Ebstein malformation of the tricuspid valve|Morphological anomaly|1|27","254892|Autosomal dominant progressive external ophthalmoplegia|Disease|5|81","273|Steinert myotonic dystrophy|Disease|0|108","284984|Aneurysm-osteoarthritis syndrome|Disease|1|51","300751|Familial dilated cardiomyopathy with conduction defect due to LMNA mutation|Disease|1|17","31826|Ethylene glycol poisoning|Disease|0|44","3282|Multifocal atrial tachycardia|Disease|0|25","3286|Catecholaminergic polymorphic ventricular tachycardia|Disease|7|10","330001|Wild type ATTR amyloidosis|Disease|0|32","334|Hereditary atrial fibrillation|Disease|24|11","439232|AApoAIV amyloidosis|Disease|0|30","51083|Congenital short QT syndrome|Disease|5|9","525731|Pediatric-onset Graves disease|Disease|0|48","66529|Tako-Tsubo cardiomyopathy|Disease|0|37","75249|Familial isolated restrictive cardiomyopathy|Disease|5|20","75565|Tropical endomyocardial fibrosis|Disease|0|48","97214|Eisenmenger syndrome|Malformation syndrome|0|58","976|Adenine phosphoribosyltransferase deficiency|Disease|1|18","980|Absence of the pulmonary artery|Morphological anomaly|0|37","99103|Atrial septal defect, ostium secundum type|Clinical subtype|9|35","99105|Atrial septal defect, sinus venosus type|Clinical subtype|1|27","99106|Atrial septal defect, ostium primum type|Clinical subtype|1|38"]}]}