{"context":{"query":">>hgnc>>orphanet","source_dataset":"hgnc","target_dataset":"orphanet"},"stats":{"queried":1,"total":29,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|disorder_type|gene_count|phenotype_count","mappings":[{"input":"HGNC:4827","source":"HGNC:4827|hemoglobin subunit beta","targets":["2132|Hemoglobin C disease|Disease|1|0","2133|Hemoglobin E disease|Disease|1|13","231214|Beta-thalassemia major|Disease|1|50","231222|Beta-thalassemia intermedia|Disease|1|36","231226|Unstable beta globin chain variant disease|Disease|1|49","231237|Delta-beta-thalassemia|Disease|3|3","231242|Hemoglobin C-beta-thalassemia syndrome|Disease|1|4","231249|Hemoglobin E-beta-thalassemia syndrome|Disease|1|4","232|Sickle cell anemia|Disease|1|37","247511|Autosomal dominant secondary polycythemia|Disease|6|0","251365|Sickle cell S-C disease|Disease|1|0","251370|Sickle cell S-D Punjab disease|Clinical subtype|1|0","251375|Sickle cell S-E disease|Clinical subtype|1|0","251380|Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome|Disease|5|13","330041|Hemoglobin M disease|Disease|3|0","46532|Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome|Disease|4|6","695140|Sickle cell-beta zero-thalassemia|Etiological subtype|1|0","695147|Sickle cell-beta plus-thalassemia|Etiological subtype|1|0","699822|Sickle cell S-Lepore disease|Clinical subtype|2|0","700090|Sickle cell S-O Arab disease|Clinical subtype|1|0","700107|Sickle cell S-other specified hemoglobin variant|Clinical subtype|1|0","700111|Homozygous hemoglobin O Arab disease|Disease|1|0","715125|Hemoglobin E-beta-thalassemia intermedia|Clinical subtype|1|0","715128|Hemoglobin E-beta-thalassemia major|Clinical subtype|1|0","715135|Hemoglobin Lepore-beta-thalassemia intermedia|Clinical subtype|1|0","715140|Hemoglobin Lepore-beta-thalassemia major|Clinical subtype|1|0","715143|Heterozygous beta-thalassemia intermedia with supernumerary alpha-globin gene|Disease|3|0","715157|Low oxygen affinity beta chain hemoglobin disease|Etiological subtype|1|0","90039|Hemoglobin D disease|Disease|1|14"]}]}