{"context":{"query":">>hgnc>>orphanet","source_dataset":"hgnc","target_dataset":"orphanet"},"stats":{"queried":1,"total":9,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|disorder_type|gene_count|phenotype_count","mappings":[{"input":"HGNC:3765","source":"HGNC:3765|fms related receptor tyrosine kinase 3","targets":["102724|Acute myeloid leukemia with t(8;21)(q22;q22) translocation|Disease|5|0","585909|B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)|Etiological subtype|7|0","589534|Mixed phenotype acute leukemia with t(9;22)(q34.1;q11.2)|Etiological subtype|2|0","589595|Mixed phenotype acute leukemia with t(v;11q23.3)|Etiological subtype|3|0","98829|Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)|Disease|4|0","98832|Acute myeloid leukemia with minimal differentiation|Disease|1|0","98833|Acute myeloblastic leukemia without maturation|Disease|2|0","98834|Acute myeloblastic leukemia with maturation|Disease|3|0","99861|Precursor T-cell acute lymphoblastic leukemia|Disease|23|0"]}]}