{"context":{"query":">>hgnc>>gencc","source_dataset":"hgnc","target_dataset":"gencc"},"stats":{"queried":1,"total":16,"mapped":1},"pagination":{"has_next":false},"schema":"id|gene_symbol|disease_title|classification_title|moi_title|submitter_title","mappings":[{"input":"HGNC:15979","source":"HGNC:15979|tumor protein p63","targets":["GENCC_000101-HGNC_15979-MONDO_0957216-HP_0000006-GENCC_100003|TP63|premature ovarian failure 21|Moderate|Autosomal dominant|Ambry Genetics","GENCC_000101-HGNC_15979-OMIM_604292-HP_0000006-GENCC_100001|TP63|ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3|Definitive|Autosomal dominant|Ambry Genetics","GENCC_000105-HGNC_15979-MONDO_0011535-HP_0000006-GENCC_100003|TP63|split hand-foot malformation 4|Moderate|Autosomal dominant|Illumina","GENCC_000106-HGNC_15979-OMIM_604292-HP_0000006-GENCC_100002|TP63|ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000106-HGNC_15979-OMIM_620311-HP_0000006-GENCC_100002|TP63|premature ovarian failure 21|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000110-HGNC_15979-ORPHANET_1071-HP_0000006-GENCC_100009|TP63|ankyloblepharon-ectodermal defects-cleft lip/palate syndrome|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_15979-ORPHANET_1896-HP_0000006-GENCC_100009|TP63|EEC syndrome|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_15979-ORPHANET_2440-HP_0000006-GENCC_100009|TP63|split hand-foot malformation|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_15979-ORPHANET_69085-HP_0000006-GENCC_100009|TP63|limb-mammary syndrome|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_15979-ORPHANET_978-HP_0000006-GENCC_100009|TP63|ADULT syndrome|Supportive|Autosomal dominant|Orphanet","GENCC_000111-HGNC_15979-MONDO_1040001-HP_0000006-GENCC_100002|TP63|TP63-related ectodermal dysplasia spectrum with limb and orofacial malformations|Strong|Autosomal dominant|PanelApp Australia","GENCC_000112-HGNC_15979-MONDO_0007508-HP_0000006-GENCC_100001|TP63|Rapp-Hodgkin syndrome|Definitive|Autosomal dominant|G2P","GENCC_000112-HGNC_15979-OMIM_103285-HP_0000006-GENCC_100001|TP63|ADULT syndrome|Definitive|Autosomal dominant|G2P","GENCC_000112-HGNC_15979-OMIM_106260-HP_0000006-GENCC_100001|TP63|ankyloblepharon-ectodermal defects-cleft lip/palate syndrome|Definitive|Autosomal dominant|G2P","GENCC_000112-HGNC_15979-OMIM_129400-HP_0000006-GENCC_100001|TP63|Rapp-Hodgkin syndrome|Definitive|Autosomal dominant|G2P","GENCC_000112-HGNC_15979-OMIM_603543-HP_0000006-GENCC_100001|TP63|limb-mammary syndrome|Definitive|Autosomal dominant|G2P"]}]}