{"context":{"query":">>hgnc>>orphanet","source_dataset":"hgnc","target_dataset":"orphanet"},"stats":{"queried":1,"total":9,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|disorder_type|gene_count|phenotype_count","mappings":[{"input":"HGNC:6697","source":"HGNC:6697|LDL receptor related protein 5","targets":["178377|Osteosclerosis-developmental delay-craniosynostosis syndrome|Malformation syndrome|1|16","2783|Autosomal dominant osteopetrosis type 1|Malformation syndrome|1|0","2788|Osteoporosis-pseudoglioma syndrome|Disease|1|34","2790|Endosteal hyperostosis, Worth type|Malformation syndrome|1|13","2924|Isolated polycystic liver disease|Malformation syndrome|4|22","3416|Hyperostosis corticalis generalisata|Malformation syndrome|2|8","498481|LRP5-related primary osteoporosis|Malformation syndrome|2|0","891|Familial exudative vitreoretinopathy|Disease|6|27","90050|Retinopathy of prematurity|Disease|3|15"]}]}