{"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:7765","source":"HGNC:7765|neurofibromin 1","targets":["139474|17q11.2 microduplication syndrome|Malformation syndrome|1|16","29072|Hereditary pheochromocytoma-paraganglioma|Disease|15|41","293199|Pleomorphic rhabdomyosarcoma|Clinical subtype|2|0","363700|Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion|Etiological subtype|1|71","638|Neurofibromatosis-Noonan syndrome|Malformation syndrome|2|18","86834|Juvenile myelomonocytic leukemia|Disease|6|0","97685|17q11 microdeletion syndrome|Clinical subtype|1|94","99756|Alveolar rhabdomyosarcoma|Clinical subtype|5|0","99757|Embryonal rhabdomyosarcoma|Clinical subtype|4|0"]}]}