{"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:7989","source":"HGNC:7989|NRAS proto-oncogene, GTPase","targets":["146|Differentiated thyroid carcinoma|Disease|29|0","2612|Linear nevus sebaceus syndrome|Disease|3|31","268114|RAS-associated autoimmune leukoproliferative disease|Disease|2|0","389|Langerhans cell histiocytosis|Disease|3|27","626|Large/giant congenital melanocytic nevus|Disease|7|21","648|Noonan syndrome|Malformation syndrome|15|70","86834|Juvenile myelomonocytic leukemia|Disease|6|0"]}]}