{"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:11364","source":"HGNC:11364|signal transducer and activator of transcription 3","targets":["2314|Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency|Disease|1|49","438159|STAT3-related early-onset multisystem autoimmune disease|Disease|1|0","512017|Chronic lymphoproliferative disorder of natural killer cells|Disease|1|0","520|Acute promyelocytic leukemia|Disease|13|36","667662|Breast implant-associated anaplastic large cell lymphoma|Disease|7|0","86872|T-cell large granular lymphocyte leukemia|Disease|1|0","99885|Isolated permanent neonatal diabetes mellitus|Disease|6|35"]}]}