{"context":{"query":">>hgnc>>gencc","source_dataset":"hgnc","target_dataset":"gencc"},"stats":{"queried":1,"total":20,"mapped":1},"pagination":{"has_next":false},"schema":"id|gene_symbol|disease_title|classification_title|moi_title|submitter_title","mappings":[{"input":"HGNC:6697","source":"HGNC:6697|LDL receptor related protein 5","targets":["GENCC_000101-HGNC_6697-OMIM_259770-HP_0000007-GENCC_100001|LRP5|osteoporosis-pseudoglioma syndrome|Definitive|Autosomal recessive|Ambry Genetics","GENCC_000101-HGNC_6697-OMIM_601813-HP_0032113-GENCC_100001|LRP5|exudative vitreoretinopathy 4|Definitive|Semidominant|Ambry Genetics","GENCC_000101-HGNC_6697-OMIM_607634-HP_0000006-GENCC_100003|LRP5|autosomal dominant osteopetrosis 1|Moderate|Autosomal dominant|Ambry Genetics","GENCC_000104-HGNC_6697-OMIM_144750-HP_0000006-GENCC_100002|LRP5|autosomal dominant osteosclerosis, Worth type|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000104-HGNC_6697-OMIM_617875-HP_0000006-GENCC_100002|LRP5|polycystic liver disease 4 with or without kidney cysts|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000106-HGNC_6697-OMIM_144750-HP_0000006-GENCC_100002|LRP5|autosomal dominant osteosclerosis, Worth type|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000106-HGNC_6697-OMIM_259770-HP_0000007-GENCC_100002|LRP5|osteoporosis-pseudoglioma syndrome|Strong|Autosomal recessive|Labcorp Genetics (formerly Invitae)","GENCC_000106-HGNC_6697-OMIM_601813-HP_0000006-GENCC_100002|LRP5|exudative vitreoretinopathy 4|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000106-HGNC_6697-OMIM_617875-HP_0000006-GENCC_100002|LRP5|polycystic liver disease 4 with or without kidney cysts|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000107-HGNC_6697-OMIM_601813-HP_0000005-GENCC_100002|LRP5|exudative vitreoretinopathy 4|Strong|Unknown|Laboratory for Molecular Medicine","GENCC_000110-HGNC_6697-ORPHANET_178377-HP_0000006-GENCC_100009|LRP5|osteosclerosis-developmental delay-craniosynostosis syndrome|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_6697-ORPHANET_2783-HP_0000006-GENCC_100009|LRP5|autosomal dominant osteopetrosis 1|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_6697-ORPHANET_2788-HP_0000007-GENCC_100009|LRP5|osteoporosis-pseudoglioma syndrome|Supportive|Autosomal recessive|Orphanet","GENCC_000110-HGNC_6697-ORPHANET_2790-HP_0000006-GENCC_100009|LRP5|autosomal dominant osteosclerosis, Worth type|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_6697-ORPHANET_2924-HP_0000006-GENCC_100009|LRP5|polycystic liver disease 1|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_6697-ORPHANET_3416-HP_0000006-GENCC_100009|LRP5|hyperostosis corticalis generalisata|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_6697-ORPHANET_891-HP_0000006-GENCC_100009|LRP5|exudative vitreoretinopathy|Supportive|Autosomal dominant|Orphanet","GENCC_000112-HGNC_6697-OMIM_259770-HP_0000007-GENCC_100001|LRP5|osteoporosis-pseudoglioma syndrome|Definitive|Autosomal recessive|G2P","GENCC_000112-HGNC_6697-OMIM_601813-HP_0000006-GENCC_100001|LRP5|exudative vitreoretinopathy 4|Definitive|Autosomal dominant|G2P","GENCC_000112-HGNC_6697-OMIM_601884-HP_0000006-GENCC_100001|LRP5|bone mineral density quantitative trait locus 1|Definitive|Autosomal dominant|G2P"]}]}