{"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:6990","source":"HGNC:6990|methyl-CpG binding protein 2","targets":["GENCC_000101-HGNC_6990-OMIM_312750-HP_0001417-GENCC_100001|MECP2|Rett syndrome|Definitive|X-linked|Ambry Genetics","GENCC_000106-HGNC_6990-OMIM_312750-HP_0001417-GENCC_100002|MECP2|Rett syndrome|Strong|X-linked|Labcorp Genetics (formerly Invitae)","GENCC_000110-HGNC_6990-ORPHANET_209370-HP_0001417-GENCC_100009|MECP2|severe neonatal-onset encephalopathy with microcephaly|Supportive|X-linked|Orphanet","GENCC_000110-HGNC_6990-ORPHANET_3077-HP_0001417-GENCC_100009|MECP2|X-linked intellectual disability-psychosis-macroorchidism syndrome|Supportive|X-linked|Orphanet","GENCC_000110-HGNC_6990-ORPHANET_3095-HP_0000006-GENCC_100009|MECP2|atypical Rett syndrome|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_6990-ORPHANET_536-HP_0000005-GENCC_100009|MECP2|systemic lupus erythematosus|Supportive|Unknown|Orphanet","GENCC_000110-HGNC_6990-ORPHANET_777-HP_0001417-GENCC_100009|MECP2|non-syndromic X-linked intellectual disability|Supportive|X-linked|Orphanet","GENCC_000110-HGNC_6990-ORPHANET_778-HP_0001417-GENCC_100009|MECP2|Rett syndrome|Supportive|X-linked|Orphanet","GENCC_000112-HGNC_6990-OMIM_300260-HP_0001417-GENCC_100001|MECP2|syndromic X-linked intellectual disability Lubs type|Definitive|X-linked|G2P","GENCC_000112-HGNC_6990-OMIM_300673-HP_0001417-GENCC_100001|MECP2|severe neonatal-onset encephalopathy with microcephaly|Definitive|X-linked|G2P","GENCC_000112-HGNC_6990-OMIM_300815-HP_0001417-GENCC_100001|MECP2|chromosome Xq28 duplication syndrome|Definitive|X-linked|G2P","GENCC_000112-HGNC_6990-OMIM_312750-HP_0001417-GENCC_100001|MECP2|Rett syndrome|Definitive|X-linked|G2P"]}]}