{"context":{"query":">>hgnc>>gencc","source_dataset":"hgnc","target_dataset":"gencc"},"stats":{"queried":1,"total":4,"mapped":1},"pagination":{"has_next":false},"schema":"id|gene_symbol|disease_title|classification_title|moi_title|submitter_title","mappings":[{"input":"HGNC:76","source":"HGNC:76|ABL proto-oncogene 1, non-receptor tyrosine kinase","targets":["GENCC_000101-HGNC_76-MONDO_0005497-HP_0000007-GENCC_100004|ABL1|bone development disease|Limited|Autosomal recessive|Ambry Genetics","GENCC_000104-HGNC_76-MONDO_0003900-HP_0000006-GENCC_100003|ABL1|connective tissue disorder|Moderate|Autosomal dominant|Genomics England PanelApp","GENCC_000106-HGNC_76-OMIM_617602-HP_0000006-GENCC_100002|ABL1|congenital heart defects and skeletal malformations syndrome|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000112-HGNC_76-OMIM_617602-HP_0000006-GENCC_100002|ABL1|congenital heart defects and skeletal malformations syndrome|Strong|Autosomal dominant|G2P"]}]}