{"context":{"query":">>hgnc>>orphanet","source_dataset":"hgnc","target_dataset":"orphanet"},"stats":{"queried":1,"total":9,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|disorder_type|gene_count|phenotype_count","mappings":[{"input":"HGNC:15979","source":"HGNC:15979|tumor protein p63","targets":["1072|Ankyloblepharon filiforme adnatum-cleft palate syndrome|Clinical subtype|1|5","141291|Cleft lip and alveolus|Morphological anomaly|4|12","1896|EEC syndrome|Malformation syndrome|1|61","199302|Isolated cleft lip|Morphological anomaly|4|19","199306|Cleft lip/palate|Morphological anomaly|13|21","2440|Isolated split hand-split foot malformation|Malformation syndrome|8|8","69085|Limb-mammary syndrome|Malformation syndrome|1|32","93930|Classic bladder exstrophy|Clinical subtype|2|13","978|ADULT syndrome|Malformation syndrome|1|24"]}]}