{"context":{"query":">>hgnc>>orphanet","source_dataset":"hgnc","target_dataset":"orphanet"},"stats":{"queried":1,"total":6,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|disorder_type|gene_count|phenotype_count","mappings":[{"input":"HGNC:8803","source":"HGNC:8803|platelet derived growth factor receptor alpha","targets":["168940|Chronic eosinophilic leukemia|Disease|2|0","168947|Myeloid/lymphoid neoplasm associated with PDGFRA rearrangement|Disease|1|0","199306|Cleft lip/palate|Morphological anomaly|13|21","314950|Primary hypereosinophilic syndrome|Disease|5|0","44890|Gastrointestinal stromal tumor|Disease|7|18","585877|B-lymphoblastic leukemia/lymphoma with recurrent genetic abnormality|Etiological subtype|2|0"]}]}