{"context":{"query":">>hgnc>>orphanet","source_dataset":"hgnc","target_dataset":"orphanet"},"stats":{"queried":1,"total":12,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|disorder_type|gene_count|phenotype_count","mappings":[{"input":"HGNC:1101","source":"HGNC:1101|BRCA2 DNA repair associated","targets":["1331|Familial prostate cancer|Disease|15|0","1333|Familial pancreatic carcinoma|Disease|9|24","145|Hereditary breast and/or ovarian cancer syndrome|Disease|15|7","178|Chordoma|Disease|3|0","227535|Hereditary breast cancer|Disease|10|0","319462|Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations|Disease|1|0","440437|Familial colorectal cancer Type X|Disease|10|53","654|Nephroblastoma|Disease|12|27","667662|Breast implant-associated anaplastic large cell lymphoma|Disease|7|0","694963|Inflammatory breast cancer|Disease|2|0","70567|Cholangiocarcinoma|Disease|4|8","84|Fanconi anemia|Malformation syndrome|23|106"]}]}