{"context":{"query":">>hgnc>>orphanet","source_dataset":"hgnc","target_dataset":"orphanet"},"stats":{"queried":1,"total":15,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|disorder_type|gene_count|phenotype_count","mappings":[{"input":"HGNC:8975","source":"HGNC:8975|phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha","targets":["140944|CLOVES syndrome|Malformation syndrome|1|43","144|Lynch syndrome|Disease|9|62","168984|CLAPO syndrome|Malformation syndrome|1|20","201|Cowden syndrome|Clinical subtype|9|57","210159|Adult hepatocellular carcinoma|Disease|9|0","221061|Familial cerebral cavernous malformation|Malformation syndrome|4|25","2495|Meningioma|Disease|12|74","276280|Hemihyperplasia-multiple lipomatosis syndrome|Malformation syndrome|1|19","295239|Macrodactyly of fingers, unilateral|Clinical subtype|1|0","295243|Macrodactyly of toes, unilateral|Clinical subtype|1|0","314662|Segmental progressive overgrowth syndrome with fibroadipose hyperplasia|Disease|1|14","60040|Megalencephaly-capillary malformation-polymicrogyria syndrome|Malformation syndrome|1|35","714737|Diffuse capillary malformation with overgrowth|Morphological anomaly|2|0","90308|Capillary-lymphatic-venous malformation with segmental distribution|Disease|2|31","99802|Hemimegalencephaly|Malformation syndrome|3|33"]}]}