{"context":{"query":">>hgnc>>orphanet","source_dataset":"hgnc","target_dataset":"orphanet"},"stats":{"queried":1,"total":6,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|disorder_type|gene_count|phenotype_count","mappings":[{"input":"HGNC:1884","source":"HGNC:1884|CF transmembrane conductance regulator","targets":["399805|Male infertility with azoospermia or oligozoospermia due to single gene mutation|Disease|37|7","48|Congenital bilateral absence of vas deferens|Morphological anomaly|2|7","498359|Aquagenic palmoplantar keratoderma|Disease|1|12","586|Cystic fibrosis|Disease|19|35","60033|Idiopathic bronchiectasis|Disease|4|19","700124|Autosomal recessive hereditary chronic pancreatitis|Disease|2|0"]}]}