{"context":{"query":">>hgnc>>hpo","source_dataset":"hgnc","target_dataset":"hpo"},"stats":{"queried":1,"total":23,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|definition","mappings":[{"input":"HGNC:1777","source":"HGNC:1777|cyclin dependent kinase 6","targets":["HP:0000007|Autosomal recessive inheritance|","HP:0000076|Vesicoureteral reflux|","HP:0000122|Unilateral renal agenesis|","HP:0000219|Thin upper lip vermilion|","HP:0000252|Microcephaly|","HP:0000340|Sloping forehead|","HP:0000582|Upslanted palpebral fissure|","HP:0001250|Seizure|","HP:0001256|Mild intellectual disability|","HP:0001263|Global developmental delay|","HP:0001274|Agenesis of corpus callosum|","HP:0001302|Pachygyria|","HP:0001347|Hyperreflexia|","HP:0001510|Growth delay|","HP:0002119|Ventriculomegaly|","HP:0002282|Gray matter heterotopia|","HP:0003103|Abnormal cortical bone morphology|","HP:0003577|Congenital onset|","HP:0004322|Short stature|","HP:0007333|Hypoplasia of the frontal lobes|","HP:0009879|Simplified gyral pattern|","HP:0010864|Severe intellectual disability|","HP:0011451|Primary microcephaly|"]}]}