{"context":{"query":">>hgnc>>gencc","source_dataset":"hgnc","target_dataset":"gencc"},"stats":{"queried":2,"total":15,"mapped":2},"pagination":{"has_next":false},"schema":"id|gene_symbol|disease_title|classification_title|moi_title|submitter_title","mappings":[{"input":"HGNC:11909","source":"HGNC:11909|TNF receptor superfamily member 11b","targets":["GENCC_000106-HGNC_11909-OMIM_239000-HP_0000007-GENCC_100002|TNFRSF11B|juvenile Paget disease|Strong|Autosomal recessive|Labcorp Genetics (formerly Invitae)","GENCC_000110-HGNC_11909-ORPHANET_2801-HP_0000007-GENCC_100009|TNFRSF11B|juvenile Paget disease|Supportive|Autosomal recessive|Orphanet","GENCC_000111-HGNC_11909-OMIM_239000-HP_0000007-GENCC_100002|TNFRSF11B|juvenile Paget disease|Strong|Autosomal recessive|PanelApp Australia"]},{"input":"HGNC:11908","source":"HGNC:11908|TNF receptor superfamily member 11a","targets":["GENCC_000101-HGNC_11908-MONDO_0009138-HP_0000007-GENCC_100004|TNFRSF11A|dysosteosclerosis|Limited|Autosomal recessive|Ambry Genetics","GENCC_000101-HGNC_11908-OMIM_174810-HP_0000006-GENCC_100003|TNFRSF11A|familial expansile osteolysis|Moderate|Autosomal dominant|Ambry Genetics","GENCC_000101-HGNC_11908-OMIM_602080-HP_0000006-GENCC_100003|TNFRSF11A|Paget disease of bone 2, early-onset|Moderate|Autosomal dominant|Ambry Genetics","GENCC_000101-HGNC_11908-OMIM_612301-HP_0000007-GENCC_100002|TNFRSF11A|autosomal recessive osteopetrosis 7|Strong|Autosomal recessive|Ambry Genetics","GENCC_000104-HGNC_11908-MONDO_0009807-HP_0000006-GENCC_100004|TNFRSF11A|osteosarcoma|Limited|Autosomal dominant|Genomics England PanelApp","GENCC_000104-HGNC_11908-OMIM_612301-HP_0000007-GENCC_100002|TNFRSF11A|autosomal recessive osteopetrosis 7|Strong|Autosomal recessive|Genomics England PanelApp","GENCC_000106-HGNC_11908-OMIM_602080-HP_0000006-GENCC_100002|TNFRSF11A|Paget disease of bone 2, early-onset|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000106-HGNC_11908-OMIM_612301-HP_0000007-GENCC_100002|TNFRSF11A|autosomal recessive osteopetrosis 7|Strong|Autosomal recessive|Labcorp Genetics (formerly Invitae)","GENCC_000110-HGNC_11908-ORPHANET_1782-HP_0000007-GENCC_100009|TNFRSF11A|dysosteosclerosis|Supportive|Autosomal recessive|Orphanet","GENCC_000110-HGNC_11908-ORPHANET_178389-HP_0000007-GENCC_100009|TNFRSF11A|autosomal recessive osteopetrosis 7|Supportive|Autosomal recessive|Orphanet","GENCC_000110-HGNC_11908-ORPHANET_85195-HP_0000006-GENCC_100009|TNFRSF11A|familial expansile osteolysis|Supportive|Autosomal dominant|Orphanet","GENCC_000111-HGNC_11908-OMIM_612301-HP_0000007-GENCC_100002|TNFRSF11A|autosomal recessive osteopetrosis 7|Strong|Autosomal recessive|PanelApp Australia"]}]}