{"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:6407","source":"HGNC:6407|KRAS proto-oncogene, GTPase","targets":["1333|Familial pancreatic carcinoma|Disease|9|24","1340|Cardiofaciocutaneous syndrome|Malformation syndrome|4|79","144|Lynch syndrome|Disease|9|62","146|Differentiated thyroid carcinoma|Disease|29|0","2396|Encephalocraniocutaneous lipomatosis|Disease|2|55","251615|Pilomyxoid astrocytoma|Histopathological subtype|8|0","2612|Linear nevus sebaceus syndrome|Disease|3|31","268114|RAS-associated autoimmune leukoproliferative disease|Disease|2|0","3339|Oculoectodermal syndrome|Malformation syndrome|1|36","648|Noonan syndrome|Malformation syndrome|15|70","86834|Juvenile myelomonocytic leukemia|Disease|6|0"]}]}