{"context":{"query":">>hgnc>>gencc","source_dataset":"hgnc","target_dataset":"gencc"},"stats":{"queried":1,"total":12,"mapped":1},"pagination":{"has_next":false},"schema":"id|gene_symbol|disease_title|classification_title|moi_title|submitter_title","mappings":[{"input":"HGNC:7029","source":"HGNC:7029|MET proto-oncogene, receptor tyrosine kinase","targets":["GENCC_000101-HGNC_7029-OMIM_605074-HP_0000006-GENCC_100001|MET|hereditary papillary renal cell carcinoma|Definitive|Autosomal dominant|Ambry Genetics","GENCC_000101-HGNC_7029-OMIM_607278-HP_0000006-GENCC_100004|MET|osteofibrous dysplasia|Limited|Autosomal dominant|Ambry Genetics","GENCC_000101-HGNC_7029-OMIM_616705-HP_0000007-GENCC_100004|MET|autosomal recessive nonsyndromic hearing loss 97|Limited|Autosomal recessive|Ambry Genetics","GENCC_000101-HGNC_7029-OMIM_620019-HP_0000006-GENCC_100004|MET|arthrogryposis, distal, IIa 11|Limited|Autosomal dominant|Ambry Genetics","GENCC_000104-HGNC_7029-OMIM_605074-HP_0000006-GENCC_100002|MET|papillary renal cell carcinoma|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000106-HGNC_7029-OMIM_605074-HP_0000006-GENCC_100002|MET|hereditary papillary renal cell carcinoma|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000106-HGNC_7029-OMIM_616705-HP_0000007-GENCC_100002|MET|autosomal recessive nonsyndromic hearing loss 97|Strong|Autosomal recessive|Labcorp Genetics (formerly Invitae)","GENCC_000106-HGNC_7029-OMIM_620019-HP_0000005-GENCC_100004|MET|arthrogryposis, distal, IIa 11|Limited|Unknown|Labcorp Genetics (formerly Invitae)","GENCC_000110-HGNC_7029-ORPHANET_47044-HP_0000006-GENCC_100009|MET|papillary renal cell carcinoma|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_7029-ORPHANET_488265-HP_0000006-GENCC_100009|MET|osteofibrous dysplasia|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_7029-ORPHANET_90636-HP_0000007-GENCC_100009|MET|hearing loss, autosomal recessive|Supportive|Autosomal recessive|Orphanet","GENCC_000112-HGNC_7029-OMIM_605074-HP_0000006-GENCC_100001|MET|hereditary papillary renal cell carcinoma|Definitive|Autosomal dominant|G2P"]}]}