{"context":{"query":">>hgnc>>orphanet","source_dataset":"hgnc","target_dataset":"orphanet"},"stats":{"queried":1,"total":10,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|disorder_type|gene_count|phenotype_count","mappings":[{"input":"HGNC:9967","source":"HGNC:9967|ret proto-oncogene","targets":["146|Differentiated thyroid carcinoma|Disease|29|0","1848|Renal agenesis, bilateral|Clinical subtype|6|18","247698|Multiple endocrine neoplasia type 2A|Clinical subtype|1|0","247709|Multiple endocrine neoplasia type 2B|Clinical subtype|1|0","276621|Sporadic pheochromocytoma/secreting paraganglioma|Disease|6|36","29072|Hereditary pheochromocytoma-paraganglioma|Disease|15|41","388|Hirschsprung disease|Disease|14|19","93100|Renal agenesis, unilateral|Clinical subtype|8|0","99361|Isolated familial medullary thyroid carcinoma|Disease|3|0","99803|Haddad syndrome|Malformation syndrome|3|19"]}]}