{"context":{"query":">>hgnc>>orphanet","source_dataset":"hgnc","target_dataset":"orphanet"},"stats":{"queried":1,"total":4,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|disorder_type|gene_count|phenotype_count","mappings":[{"input":"HGNC:76","source":"HGNC:76|ABL proto-oncogene 1, non-receptor tyrosine kinase","targets":["521|Chronic myeloid leukemia|Disease|3|11","585909|B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)|Etiological subtype|7|0","643503|Marfanoid habitus-facial dysmorphism-skeletal abnormality-heart defect syndrome|Disease|1|0","99861|Precursor T-cell acute lymphoblastic leukemia|Disease|23|0"]}]}