{"context":{"query":">>hgnc>>orphanet","source_dataset":"hgnc","target_dataset":"orphanet"},"stats":{"queried":1,"total":8,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|disorder_type|gene_count|phenotype_count","mappings":[{"input":"HGNC:10593","source":"HGNC:10593|sodium voltage-gated channel alpha subunit 5","targets":["101016|Romano-Ward syndrome|Disease|19|13","130|Brugada syndrome|Disease|22|12","1344|Isolated atrial standstill|Disease|2|32","154|Familial isolated dilated cardiomyopathy|Disease|53|13","166282|Hereditary sick sinus syndrome|Disease|4|0","228140|Idiopathic ventricular fibrillation|Disease|2|0","334|Hereditary atrial fibrillation|Disease|24|11","871|Hereditary progressive cardiac conduction defect|Disease|4|8"]}]}