{"context":{"query":">>hgnc>>orphanet","source_dataset":"hgnc","target_dataset":"orphanet"},"stats":{"queried":1,"total":11,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|disorder_type|gene_count|phenotype_count","mappings":[{"input":"HGNC:1097","source":"HGNC:1097|B-Raf proto-oncogene, serine/threonine kinase","targets":["1340|Cardiofaciocutaneous syndrome|Malformation syndrome|4|79","146|Differentiated thyroid carcinoma|Disease|29|0","251615|Pilomyxoid astrocytoma|Histopathological subtype|8|0","389|Langerhans cell histiocytosis|Disease|3|27","500|Noonan syndrome with multiple lentigines|Malformation syndrome|3|50","54595|Craniopharyngioma|Disease|2|46","58017|Classic hairy cell leukemia|Disease|1|0","626|Large/giant congenital melanocytic nevus|Disease|7|21","648|Noonan syndrome|Malformation syndrome|15|70","840|Syringocystadenoma papilliferum|Disease|1|5","96253|Cushing disease|Disease|7|64"]}]}