{"context":{"query":">>hgnc>>orphanet","source_dataset":"hgnc","target_dataset":"orphanet"},"stats":{"queried":1,"total":7,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|disorder_type|gene_count|phenotype_count","mappings":[{"input":"HGNC:7577","source":"HGNC:7577|myosin heavy chain 7","targets":["154|Familial isolated dilated cardiomyopathy|Disease|53|13","1880|Ebstein malformation of the tricuspid valve|Morphological anomaly|1|27","324604|Classic multiminicore myopathy|Clinical subtype|3|29","54260|Left ventricular noncompaction|Disease|15|0","59135|Laing distal myopathy|Disease|1|20","636965|Autosomal dominant myosin storage myopathy|Clinical subtype|1|0","636970|Autosomal recessive myosin storage myopathy|Clinical subtype|1|0"]}]}