{"context":{"query":">>hgnc>>gencc","source_dataset":"hgnc","target_dataset":"gencc"},"stats":{"queried":1,"total":25,"mapped":1},"pagination":{"has_next":false},"schema":"id|gene_symbol|disease_title|classification_title|moi_title|submitter_title","mappings":[{"input":"HGNC:4827","source":"HGNC:4827|hemoglobin subunit beta","targets":["GENCC_000101-HGNC_4827-OMIM_613985-HP_0032113-GENCC_100001|HBB|beta-thalassemia HBB/LCRB|Definitive|Semidominant|Ambry Genetics","GENCC_000101-HGNC_4827-OMIM_617971-HP_0000006-GENCC_100003|HBB|hemoglobin M disease|Moderate|Autosomal dominant|Ambry Genetics","GENCC_000104-HGNC_4827-OMIM_617980-HP_0000006-GENCC_100002|HBB|erythrocytosis, familial, 6|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000106-HGNC_4827-OMIM_140700-HP_0000006-GENCC_100002|HBB|Heinz body anemia|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000106-HGNC_4827-OMIM_603902-HP_0000006-GENCC_100002|HBB|dominant beta-thalassemia|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000106-HGNC_4827-OMIM_603903-HP_0000007-GENCC_100002|HBB|sickle cell disease|Strong|Autosomal recessive|Labcorp Genetics (formerly Invitae)","GENCC_000106-HGNC_4827-OMIM_613985-HP_0000007-GENCC_100002|HBB|beta-thalassemia HBB/LCRB|Strong|Autosomal recessive|Labcorp Genetics (formerly Invitae)","GENCC_000106-HGNC_4827-OMIM_617980-HP_0000006-GENCC_100002|HBB|erythrocytosis, familial, 6|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000108-HGNC_4827-MONDO_0019402-HP_0000007-GENCC_100001|HBB|beta thalassemia|Definitive|Autosomal recessive|Myriad Women’s Health","GENCC_000110-HGNC_4827-ORPHANET_2132-HP_0000007-GENCC_100009|HBB|hemoglobin C disease|Supportive|Autosomal recessive|Orphanet","GENCC_000110-HGNC_4827-ORPHANET_2133-HP_0000007-GENCC_100009|HBB|hemoglobin E disease|Supportive|Autosomal recessive|Orphanet","GENCC_000110-HGNC_4827-ORPHANET_231214-HP_0000007-GENCC_100009|HBB|beta-thalassemia major|Supportive|Autosomal recessive|Orphanet","GENCC_000110-HGNC_4827-ORPHANET_231222-HP_0000007-GENCC_100009|HBB|beta-thalassemia intermedia|Supportive|Autosomal recessive|Orphanet","GENCC_000110-HGNC_4827-ORPHANET_231226-HP_0000006-GENCC_100009|HBB|dominant beta-thalassemia|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_4827-ORPHANET_231237-HP_0000007-GENCC_100009|HBB|delta-beta-thalassemia|Supportive|Autosomal recessive|Orphanet","GENCC_000110-HGNC_4827-ORPHANET_231242-HP_0000007-GENCC_100009|HBB|hemoglobin C-beta-thalassemia syndrome|Supportive|Autosomal recessive|Orphanet","GENCC_000110-HGNC_4827-ORPHANET_231249-HP_0000007-GENCC_100009|HBB|hemoglobin E-beta-thalassemia syndrome|Supportive|Autosomal recessive|Orphanet","GENCC_000110-HGNC_4827-ORPHANET_232-HP_0000007-GENCC_100009|HBB|sickle cell disease|Supportive|Autosomal recessive|Orphanet","GENCC_000110-HGNC_4827-ORPHANET_251359-HP_0000007-GENCC_100009|HBB|sickle cell-beta-thalassemia disease syndrome|Supportive|Autosomal recessive|Orphanet","GENCC_000110-HGNC_4827-ORPHANET_251365-HP_0000007-GENCC_100009|HBB|sickle cell-hemoglobin c disease syndrome|Supportive|Autosomal recessive|Orphanet","GENCC_000110-HGNC_4827-ORPHANET_251370-HP_0000007-GENCC_100009|HBB|sickle cell-hemoglobin d disease syndrome|Supportive|Autosomal recessive|Orphanet","GENCC_000110-HGNC_4827-ORPHANET_251375-HP_0000007-GENCC_100009|HBB|sickle cell-hemoglobin E disease syndrome|Supportive|Autosomal recessive|Orphanet","GENCC_000110-HGNC_4827-ORPHANET_251380-HP_0000007-GENCC_100009|HBB|hereditary persistence of fetal hemoglobin-sickle cell disease syndrome|Supportive|Autosomal recessive|Orphanet","GENCC_000110-HGNC_4827-ORPHANET_330041-HP_0000006-GENCC_100009|HBB|hemoglobin M disease|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_4827-ORPHANET_46532-HP_0000006-GENCC_100009|HBB|hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome|Supportive|Autosomal dominant|Orphanet"]}]}