{"context":{"query":">>hpo>>orphanet","source_dataset":"hpo","target_dataset":"orphanet"},"stats":{"queried":1,"total":81,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|disorder_type|gene_count|phenotype_count","mappings":[{"input":"HP:0001297","source":"HP:0001297|Stroke","targets":["100006|ABeta amyloidosis, Dutch type|Clinical subtype|1|10","100008|ACys amyloidosis|Clinical subtype|1|5","100070|Progressive non-fluent aphasia|Disease|8|32","1054|Aneurysm of sinus of Valsalva|Morphological anomaly|0|11","1163|Aspergillosis|Disease|0|56","1359|Carney complex|Disease|2|64","136|Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy|Disease|1|40","140989|Primary angiitis of the central nervous system|Disease|0|30","1457|Coarctation of aorta|Morphological anomaly|0|18","1478|Interatrial communication|Morphological anomaly|0|19","1560|Cysticercosis|Disease|0|49","167635|Scleromyxedema|Disease|0|41","173|Cholera|Disease|0|34","1830|Schimke immuno-osseous dysplasia|Disease|1|73","1880|Ebstein malformation of the tricuspid valve|Morphological anomaly|1|27","199354|Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy|Disease|1|32","229|Familial aortic dissection|Disease|1|19","230839|Classical-like Ehlers-Danlos syndrome type 1|Disease|1|20","2637|Microcephalic osteodysplastic primordial dwarfism type II|Malformation syndrome|1|52","268943|Unilateral polymicrogyria|Morphological anomaly|0|37","275761|Lysosomal acid lipase deficiency|Disease|0|49","3077|X-linked intellectual disability-psychosis-macroorchidism syndrome|Malformation syndrome|1|27","320|Apparent mineralocorticoid excess|Disease|1|17","3205|Sturge-Weber syndrome|Malformation syndrome|1|51","324|Fabry disease|Disease|1|76","324703|ABetaL34V amyloidosis|Clinical subtype|1|11","324708|ABeta amyloidosis, Iowa type|Clinical subtype|1|9","324713|ABeta amyloidosis, Italian type|Clinical subtype|1|7","3287|Takayasu arteritis|Disease|3|54","33226|Waldenström macroglobulinemia|Disease|1|45","3325|Classic heparin-induced thrombocytopenia|Disease|0|15","33475|Meningococcal meningitis|Disease|0|35","363705|Craniofaciofrontodigital syndrome|Disease|0|69","395|Homocystinuria due to methylene tetrahydrofolate reductase deficiency|Disease|1|50","401945|Moyamoya disease with early-onset achalasia|Disease|1|8","444463|Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome due to TPP2 deficiency|Disease|1|14","447|Paroxysmal nocturnal hemoglobinuria|Disease|1|44","449285|Snakebite envenomation|Disease|0|34","464343|Catastrophic antiphospholipid syndrome|Disease|0|52","466677|Scorpion envenomation|Disease|0|58","480864|Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome|Disease|1|51","494424|Extracranial carotid artery aneurysm|Morphological anomaly|0|28","49827|Thiamine-responsive megaloblastic anemia syndrome|Disease|1|20","51608|Generalized arterial calcification of infancy|Disease|2|60","533|Listeriosis|Disease|0|68","536467|B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome|Clinical subtype|1|83","54057|Thrombotic thrombocytopenic purpura|Disease|0|22","542310|Leukoencephalopathy with calcifications and cysts|Disease|1|27","557003|Oculoskeletodental syndrome|Disease|1|38","66631|CEDNIK syndrome|Disease|1|33","729|Polycythemia vera|Disease|1|35","739|Prader-Willi syndrome|Disease|0|90","740|Hutchinson-Gilford progeria syndrome|Disease|2|93","75249|Familial isolated restrictive cardiomyopathy|Disease|5|20","758|Pseudoxanthoma elasticum|Disease|2|41","760|Purine nucleoside phosphorylase deficiency|Disease|1|29","786|Generalized glucocorticoid resistance syndrome|Disease|1|21","79282|Methylmalonic acidemia with homocystinuria, type cblC|Clinical subtype|1|76","79312|Vitamin B12-unresponsive methylmalonic acidemia type mut-|Clinical subtype|1|29","85451|ATTRV122I amyloidosis|Clinical subtype|1|25","892|Von Hippel-Lindau disease|Disease|2|41","90041|Gaisböck syndrome|Disease|0|36","90064|Acute peripheral arterial occlusion|Particular clinical situation in a disease or syndrome|0|17","90289|Localized scleroderma|Disease|0|55","90324|Cockayne syndrome type 3|Clinical subtype|2|74","904|Williams syndrome|Malformation syndrome|18|186","911|Combined immunodeficiency due to ZAP70 deficiency|Disease|1|30","91139|Simple cryoglobulinemia|Disease|0|55","91387|Familial thoracic aortic aneurysm and aortic dissection|Disease|20|42","927|Hyperammonemia due to N-acetylglutamate synthase deficiency|Disease|1|42","93585|Immune-mediated thrombotic thrombocytopenic purpura|Clinical subtype|0|41","93598|Primary hyperoxaluria type 1|Clinical subtype|1|19","95409|Acute adrenal insufficiency|Clinical syndrome|0|44","96253|Cushing disease|Disease|7|64","97214|Eisenmenger syndrome|Malformation syndrome|0|58","97339|Dural sinus malformation with arteriovenous shunt|Morphological anomaly|0|48","97685|17q11 microdeletion syndrome|Clinical subtype|1|94","99103|Atrial septal defect, ostium secundum type|Clinical subtype|9|35","99104|Atrial septal defect, coronary sinus type|Clinical subtype|0|26","99105|Atrial septal defect, sinus venosus type|Clinical subtype|1|27","99889|Cushing syndrome due to ectopic ACTH secretion|Disease|0|83"]}]}