{"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:3942","source":"HGNC:3942|mechanistic target of rapamycin kinase","targets":["GENCC_000105-HGNC_3942-OMIM_616638-HP_0000006 -GENCC_100001|MTOR|macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome|Definitive|Autosomal dominant|Illumina","GENCC_000106-HGNC_3942-OMIM_616638-HP_0000006-GENCC_100002|MTOR|macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000110-HGNC_3942-ORPHANET_457485-HP_0000006-GENCC_100009|MTOR|macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome|Supportive|Autosomal dominant|Orphanet","GENCC_000112-HGNC_3942-OMIM_616638-HP_0000006-GENCC_100001|MTOR|macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome|Definitive|Autosomal dominant|G2P"]}]}