{"context":{"query":">>hgnc>>gencc","source_dataset":"hgnc","target_dataset":"gencc"},"stats":{"queried":1,"total":6,"mapped":1},"pagination":{"has_next":false},"schema":"id|gene_symbol|disease_title|classification_title|moi_title|submitter_title","mappings":[{"input":"HGNC:11179","source":"HGNC:11179|superoxide dismutase 1","targets":["GENCC_000101-HGNC_11179-OMIM_618598-HP_0000007-GENCC_100004|SOD1|spastic tetraplegia and axial hypotonia, progressive|Limited|Autosomal recessive|Ambry Genetics","GENCC_000104-HGNC_11179-OMIM_105400-HP_0000006-GENCC_100002|SOD1|amyotrophic lateral sclerosis type 1|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000106-HGNC_11179-OMIM_105400-HP_0000006-GENCC_100002|SOD1|amyotrophic lateral sclerosis type 1|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000106-HGNC_11179-OMIM_105400-HP_0000007-GENCC_100002|SOD1|amyotrophic lateral sclerosis type 1|Strong|Autosomal recessive|Labcorp Genetics (formerly Invitae)","GENCC_000106-HGNC_11179-OMIM_618598-HP_0000007-GENCC_100002|SOD1|spastic tetraplegia and axial hypotonia, progressive|Strong|Autosomal recessive|Labcorp Genetics (formerly Invitae)","GENCC_000110-HGNC_11179-ORPHANET_803-HP_0000006-GENCC_100009|SOD1|amyotrophic lateral sclerosis|Supportive|Autosomal dominant|Orphanet"]}]}