{"context":{"query":">>hgnc>>gencc","source_dataset":"hgnc","target_dataset":"gencc"},"stats":{"queried":1,"total":4,"mapped":1},"pagination":{"has_next":false},"schema":"id|gene_symbol|disease_title|classification_title|moi_title|submitter_title","mappings":[{"input":"HGNC:11110","source":"HGNC:11110|AT-rich interaction domain 1A","targets":["GENCC_000105-HGNC_11110-OMIM_614607-HP_0000006-GENCC_100002|ARID1A|intellectual disability, autosomal dominant 14|Strong|Autosomal dominant|Illumina","GENCC_000106-HGNC_11110-OMIM_614607-HP_0000006-GENCC_100002|ARID1A|intellectual disability, autosomal dominant 14|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000110-HGNC_11110-ORPHANET_1465-HP_0000006-GENCC_100009|ARID1A|Coffin-Siris syndrome|Supportive|Autosomal dominant|Orphanet","GENCC_000112-HGNC_11110-OMIM_614607-HP_0000006-GENCC_100001|ARID1A|intellectual disability, autosomal dominant 14|Definitive|Autosomal dominant|G2P"]}]}