{"context":{"query":">>hgnc>>gencc","source_dataset":"hgnc","target_dataset":"gencc"},"stats":{"queried":1,"total":7,"mapped":1},"pagination":{"has_next":false},"schema":"id|gene_symbol|disease_title|classification_title|moi_title|submitter_title","mappings":[{"input":"HGNC:8975","source":"HGNC:8975|phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha","targets":["GENCC_000101-HGNC_8975-OMIM_602501-HP_0000006-GENCC_100002|PIK3CA|megalencephaly-capillary malformation-polymicrogyria syndrome|Strong|Autosomal dominant|Ambry Genetics","GENCC_000102-HGNC_8975-MONDO_0016248-HP_0000005-GENCC_100008|PIK3CA|familial ovarian cancer|No Known Disease Relationship|Unknown|ClinGen","GENCC_000104-HGNC_8975-MONDO_0024291-HP_0000006-GENCC_100002|PIK3CA|vascular malformation|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000104-HGNC_8975-OMIM_602501-HP_0000006-GENCC_100002|PIK3CA|megalencephaly-capillary malformation-polymicrogyria syndrome|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000106-HGNC_8975-OMIM_602501-HP_0000006-GENCC_100002|PIK3CA|megalencephaly-capillary malformation-polymicrogyria syndrome|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000106-HGNC_8975-OMIM_615108-HP_0000006-GENCC_100004|PIK3CA|Cowden syndrome 5|Limited|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000110-HGNC_8975-ORPHANET_201-HP_0000006-GENCC_100009|PIK3CA|Cowden disease|Supportive|Autosomal dominant|Orphanet"]}]}