{"context":{"query":">>hgnc>>gencc","source_dataset":"hgnc","target_dataset":"gencc"},"stats":{"queried":1,"total":17,"mapped":1},"pagination":{"has_next":false},"schema":"id|gene_symbol|disease_title|classification_title|moi_title|submitter_title","mappings":[{"input":"HGNC:9588","source":"HGNC:9588|phosphatase and tensin homolog","targets":["GENCC_000101-HGNC_9588-OMIM_158350-HP_0000006-GENCC_100001|PTEN|Cowden syndrome 1|Definitive|Autosomal dominant|Ambry Genetics","GENCC_000101-HGNC_9588-OMIM_158350-HP_0000006-GENCC_100003|PTEN|Cowden syndrome 1|Moderate|Autosomal dominant|Ambry Genetics","GENCC_000101-HGNC_9588-OMIM_605309-HP_0000006-GENCC_100002|PTEN|macrocephaly-autism syndrome|Strong|Autosomal dominant|Ambry Genetics","GENCC_000101-HGNC_9588-OMIM_613028-HP_0000006-GENCC_100004|PTEN|glioma susceptibility 2|Limited|Autosomal dominant|Ambry Genetics","GENCC_000104-HGNC_9588-MONDO_0005058-HP_0000007-GENCC_100003|PTEN|leiomyosarcoma|Moderate|Autosomal recessive|Genomics England PanelApp","GENCC_000104-HGNC_9588-MONDO_0005086-HP_0000006-GENCC_100003|PTEN|renal cell carcinoma|Moderate|Autosomal dominant|Genomics England PanelApp","GENCC_000104-HGNC_9588-OMIM_158350-HP_0000006-GENCC_100002|PTEN|Cowden syndrome 1|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000104-HGNC_9588-OMIM_158350-HP_0000006-GENCC_100003|PTEN|Cowden syndrome 1|Moderate|Autosomal dominant|Genomics England PanelApp","GENCC_000104-HGNC_9588-OMIM_605309-HP_0000006-GENCC_100002|PTEN|macrocephaly-autism syndrome|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000106-HGNC_9588-OMIM_158350-HP_0000006-GENCC_100002|PTEN|Cowden syndrome 1|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000110-HGNC_9588-ORPHANET_109-HP_0000006-GENCC_100009|PTEN|Bannayan-Riley-Ruvalcaba syndrome|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_9588-ORPHANET_201-HP_0000006-GENCC_100009|PTEN|Cowden disease|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_9588-ORPHANET_210548-HP_0000006-GENCC_100009|PTEN|macrocephaly-autism syndrome|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_9588-ORPHANET_2969-HP_0000006-GENCC_100009|PTEN|Proteus-like syndrome|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_9588-ORPHANET_397596-HP_0000006-GENCC_100009|PTEN|activated PI3K-delta syndrome|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_9588-ORPHANET_65285-HP_0000006-GENCC_100009|PTEN|Lhermitte-Duclos disease|Supportive|Autosomal dominant|Orphanet","GENCC_000112-HGNC_9588-OMIM_158350-HP_0000006-GENCC_100001|PTEN|Cowden syndrome 1|Definitive|Autosomal dominant|G2P"]}]}