{"context":{"query":">>hpo>>orphanet","source_dataset":"hpo","target_dataset":"orphanet"},"stats":{"queried":1,"total":8,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|disorder_type|gene_count|phenotype_count","mappings":[{"input":"HP:0012114","source":"HP:0012114|Endometrial carcinoma","targets":["144|Lynch syndrome|Disease|9|62","157794|Hereditary mixed polyposis syndrome|Disease|2|18","201|Cowden syndrome|Clinical subtype|9|57","273|Steinert myotonic dystrophy|Disease|0|108","447877|Polymerase proofreading-related polyposis|Disease|2|7","454840|NTHL1-related polyposis|Disease|1|15","457212|Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome|Disease|1|22","90790|Congenital lipoid adrenal hyperplasia due to STAR deficency|Disease|0|25"]}]}