{"context":{"query":">>hpo>>orphanet","source_dataset":"hpo","target_dataset":"orphanet"},"stats":{"queried":1,"total":100,"mapped":1},"pagination":{"has_next":true,"next_token":"-1[]HP:0001635,74,HP:0001635,31,0]["},"schema":"id|name|disorder_type|gene_count|phenotype_count","mappings":[{"input":"HP:0001635","source":"HP:0001635|Congestive heart failure","targets":["1054|Aneurysm of sinus of Valsalva|Morphological anomaly|0|11","1055|Congenital left ventricular aneurysm|Malformation syndrome|0|6","108|Babesiosis|Disease|0|31","1194|TMEM70-related mitochondrial encephalo-cardio-myopathy|Disease|1|30","132|Hereditary butyrylcholinesterase deficiency|Disease|1|9","1329|Complete atrioventricular septal defect|Morphological anomaly|0|34","1344|Isolated atrial standstill|Disease|2|32","1345|Cardiomyopathy-cataract-hip spine disease syndrome|Disease|0|14","1349|Mitochondrial DNA-related cardiomyopathy and hearing loss|Malformation syndrome|1|30","1359|Carney complex|Disease|2|64","137608|Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome|Clinical subtype|1|19","137667|Capillary malformation-arteriovenous malformation|Clinical group|0|29","137675|Histiocytoid cardiomyopathy|Disease|1|44","139507|Dietary iron overload disease|Disease|0|25","14|Abetalipoproteinemia|Disease|1|63","141179|Non-involuting congenital hemangioma|Disease|0|12","141184|Rapidly involuting congenital hemangioma|Disease|0|14","1457|Coarctation of aorta|Morphological anomaly|0|18","1464|Univentricular heart|Morphological anomaly|0|14","1478|Interatrial communication|Morphological anomaly|0|19","154|Familial isolated dilated cardiomyopathy|Disease|53|13","157973|Congenital muscular dystrophy due to LMNA mutation|Disease|1|22","1600|Monosomy 18q syndrome|Malformation syndrome|0|65","163596|Hemoglobin Bart's fetalis syndrome|Disease|2|12","1686|Cardiac diverticulum|Morphological anomaly|0|42","171|Primary sclerosing cholangitis|Disease|4|55","183|Eosinophilic granulomatosis with polyangiitis|Disease|0|66","1830|Schimke immuno-osseous dysplasia|Disease|1|73","185|Scimitar syndrome|Malformation syndrome|0|39","1880|Ebstein malformation of the tricuspid valve|Morphological anomaly|1|27","1900|Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency|Clinical subtype|1|66","2022|Endocardial fibroelastosis|Disease|0|16","2041|Coronary arterial fistula|Morphological anomaly|0|27","206546|Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers|Disease|1|20","206569|Immune-mediated necrotizing myopathy|Disease|0|24","2108|Hallermann-Streiff syndrome|Malformation syndrome|1|50","216694|Congenitally corrected transposition of the great arteries|Morphological anomaly|0|49","217622|Sensorineural deafness with dilated cardiomyopathy|Disease|1|5","220393|Diffuse cutaneous systemic sclerosis|Clinical subtype|5|26","2299|Aortic arch interruption|Morphological anomaly|0|32","2326|Kallmann syndrome-heart disease syndrome|Malformation syndrome|0|29","2331|Kawasaki disease|Disease|0|46","2348|Familial partial lipodystrophy, Dunnigan type|Disease|1|34","2414|Congenital pulmonary lymphangiectasia|Disease|0|16","247353|Generalized pustular psoriasis|Disease|2|27","2505|Multiple benign circumferential skin creases on limbs|Disease|2|30","261519|Maternal uniparental disomy of chromosome X syndrome|Malformation syndrome|0|26","26791|Multiple acyl-CoA dehydrogenase deficiency|Disease|0|58","271861|Hereditary ATTR amyloidosis|Disease|0|36","275766|Idiopathic pulmonary arterial hypertension|Etiological subtype|0|18","276621|Sporadic pheochromocytoma/secreting paraganglioma|Disease|6|36","280365|Autosomal semi-dominant severe lipodystrophic laminopathy|Disease|1|49","29072|Hereditary pheochromocytoma-paraganglioma|Disease|15|41","300751|Familial dilated cardiomyopathy with conduction defect due to LMNA mutation|Disease|1|17","3077|X-linked intellectual disability-psychosis-macroorchidism syndrome|Malformation syndrome|1|27","3092|Fixed subaortic stenosis|Morphological anomaly|0|28","31824|Colchicine poisoning|Particular clinical situation in a disease or syndrome|0|29","31826|Ethylene glycol poisoning|Disease|0|44","324|Fabry disease|Disease|1|76","324410|X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome|Disease|1|30","324588|Familial dyskinesia and facial myokymia|Disease|1|15","324604|Classic multiminicore myopathy|Clinical subtype|3|29","3260|Idiopathic hypereosinophilic syndrome|Disease|0|78","3287|Takayasu arteritis|Disease|3|54","330001|Wild type ATTR amyloidosis|Disease|0|32","3309|Tetrasomy 5p syndrome|Malformation syndrome|0|44","33226|Waldenström macroglobulinemia|Disease|1|45","3342|Arterial tortuosity syndrome|Malformation syndrome|1|61","3385|African trypanosomiasis|Disease|0|87","3386|American trypanosomiasis|Disease|0|27","3400|Aorto-ventricular tunnel|Morphological anomaly|0|8","3403|Uhl anomaly|Morphological anomaly|0|16","34217|Naxos disease|Disease|1|14","354|GM1 gangliosidosis|Disease|0|89","35687|Erdheim-Chester disease|Disease|0|41","363618|LMNA-related cardiocutaneous progeria syndrome|Disease|1|27","363705|Craniofaciofrontodigital syndrome|Disease|0|69","367|Glycogen storage disease due to glycogen branching enzyme deficiency|Disease|0|30","391487|STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome|Disease|1|47","423461|Mucolipidosis type III alpha/beta|Clinical subtype|1|36","428|Autosomal dominant hypocalcemia|Clinical subtype|2|30","439|Isolated right ventricular hypoplasia|Morphological anomaly|0|19","444013|Combined oxidative phosphorylation defect type 23|Disease|1|27","444077|Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome|Malformation syndrome|1|79","45453|Incessant infant ventricular tachycardia|Disease|0|12","454836|Avian influenza|Disease|0|41","464|Incontinentia pigmenti|Malformation syndrome|1|67","465508|Symptomatic form of HFE-related hemochromatosis|Disease|2|44","466677|Scorpion envenomation|Disease|0|58","48818|Aceruloplasminemia|Disease|1|41","49827|Thiamine-responsive megaloblastic anemia syndrome|Disease|1|20","500533|Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome|Disease|1|34","505248|Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders|Malformation syndrome|1|71","506|Leigh syndrome|Disease|1|98","508542|Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome|Disease|1|38","52430|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia|Disease|3|43","525731|Pediatric-onset Graves disease|Disease|0|48","528|Congenital generalized lipodystrophy|Disease|0|37","53296|Familial cutaneous collagenoma|Disease|0|7","533|Listeriosis|Disease|0|68"]}]}