{"context":{"query":">>hgnc>>hpo","source_dataset":"hgnc","target_dataset":"hpo"},"stats":{"queried":1,"total":62,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|definition","mappings":[{"input":"HGNC:76","source":"HGNC:76|ABL proto-oncogene 1, non-receptor tyrosine kinase","targets":["HP:0000006|Autosomal dominant inheritance|","HP:0000028|Cryptorchidism|","HP:0000047|Hypospadias|","HP:0000218|High palate|","HP:0000233|Thin vermilion border|","HP:0000307|Pointed chin|","HP:0000319|Smooth philtrum|","HP:0000331|Short chin|","HP:0000337|Broad forehead|","HP:0000341|Narrow forehead|","HP:0000460|Narrow nose|","HP:0000490|Deeply set eye|","HP:0000582|Upslanted palpebral fissure|","HP:0000670|Carious teeth|","HP:0000678|Dental crowding|","HP:0000767|Pectus excavatum|","HP:0000776|Congenital diaphragmatic hernia|","HP:0000963|Thin skin|","HP:0000965|Cutis marmorata|","HP:0000977|Soft skin|","HP:0001166|Arachnodactyly|","HP:0001263|Global developmental delay|","HP:0001382|Joint hypermobility|","HP:0001442|Typified by somatic mosaicism|","HP:0001508|Failure to thrive|","HP:0001511|Intrauterine growth retardation|","HP:0001629|Ventricular septal defect|","HP:0001631|Atrial septal defect|","HP:0001680|Coarctation of aorta|","HP:0001744|Splenomegaly|","HP:0001763|Pes planus|","HP:0001852|Sandal gap|","HP:0001871|Abnormality of blood and blood-forming tissues|","HP:0001873|Thrombocytopenia|","HP:0001894|Thrombocytosis|","HP:0001911|Abnormal granulocyte morphology|","HP:0001912|Abnormal basophil morphology|","HP:0001945|Fever|","HP:0001974|Increased total leukocyte count|","HP:0002007|Frontal bossing|","HP:0002010|Narrow maxilla|","HP:0002023|Anal atresia|","HP:0002566|Intestinal malrotation|","HP:0002616|Aortic root aneurysm|","HP:0002650|Scoliosis|","HP:0002714|Downturned corners of mouth|","HP:0002808|Kyphosis|","HP:0003189|Long nose|","HP:0003196|Short nose|","HP:0003577|Congenital onset|","HP:0004209|Clinodactyly of the 5th finger|","HP:0004322|Short stature|","HP:0004396|Poor appetite|","HP:0004848|Ph-positive acute lymphoblastic leukemia|","HP:0004852|Reduced leukocyte alkaline phosphatase|","HP:0005506|Chronic myelogenous leukemia|","HP:0005547|Myeloproliferative disorder|","HP:0006522|Repeated pneumothoraces|","HP:0010747|Medial flaring of the eyebrow|","HP:0012378|Fatigue|","HP:0012385|Camptodactyly|","HP:0012450|Chronic constipation|"]}]}