{"context":{"query":">>hgnc>>orphanet","source_dataset":"hgnc","target_dataset":"orphanet"},"stats":{"queried":1,"total":14,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|disorder_type|gene_count|phenotype_count","mappings":[{"input":"HGNC:9588","source":"HGNC:9588|phosphatase and tensin homolog","targets":["109|Bannayan-Riley-Ruvalcaba syndrome|Clinical subtype|1|55","137608|Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome|Clinical subtype|1|19","145|Hereditary breast and/or ovarian cancer syndrome|Disease|15|7","201|Cowden syndrome|Clinical subtype|9|57","210548|Macrocephaly-intellectual disability-autism syndrome|Disease|2|24","2969|Proteus-like syndrome|Clinical subtype|1|31","494547|Squamous cell carcinoma of the hypopharynx|Disease|3|0","494550|Squamous cell carcinoma of the larynx|Disease|3|0","500464|Squamous cell carcinoma of the nasal cavity and paranasal sinuses|Disease|3|0","500478|Squamous cell carcinoma of the oropharynx|Disease|3|0","502363|Squamous cell carcinoma of the oral cavity|Disease|3|0","502366|Squamous cell carcinoma of the lip|Disease|3|0","65285|Lhermitte-Duclos disease|Clinical subtype|1|18","79076|Juvenile polyposis of infancy|Clinical subtype|2|43"]}]}