{"context":{"query":">>hgnc>>orphanet","source_dataset":"hgnc","target_dataset":"orphanet"},"stats":{"queried":1,"total":7,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|disorder_type|gene_count|phenotype_count","mappings":[{"input":"HGNC:6990","source":"HGNC:6990|methyl-CpG binding protein 2","targets":["1762|Proximal Xq28 duplication syndrome|Malformation syndrome|1|18","209370|MECP2-related severe neonatal encephalopathy|Disease|1|19","3077|X-linked intellectual disability-psychosis-macroorchidism syndrome|Malformation syndrome|1|27","3095|Atypical Rett syndrome|Disease|5|54","536|Systemic lupus erythematosus|Disease|30|44","777|X-linked non-syndromic intellectual disability|Etiological subtype|30|0","778|Rett syndrome|Disease|1|36"]}]}