{"context":{"query":">>hgnc>>hpo","source_dataset":"hgnc","target_dataset":"hpo"},"stats":{"queried":1,"total":100,"mapped":1},"pagination":{"has_next":true,"next_token":"-1[]HGNC:11766,10,HGNC:11766,58,2]["},"schema":"id|name|definition","mappings":[{"input":"HGNC:11766","source":"HGNC:11766|transforming growth factor beta 1","targets":["HP:0000006|Autosomal dominant inheritance|","HP:0000007|Autosomal recessive inheritance|","HP:0000016|Urinary retention|","HP:0000135|Hypogonadism|","HP:0000246|Sinusitis|","HP:0000303|Mandibular prognathia|","HP:0000365|Hearing impairment|","HP:0000501|Glaucoma|","HP:0000520|Proptosis|","HP:0000648|Optic atrophy|","HP:0000651|Diplopia|","HP:0000670|Carious teeth|","HP:0000684|Delayed eruption of teeth|","HP:0000716|Depression|","HP:0000739|Anxiety|","HP:0000763|Sensory neuropathy|","HP:0000787|Nephrolithiasis|","HP:0000823|Delayed puberty|","HP:0000925|Abnormality of the vertebral column|","HP:0000929|Abnormal skull morphology|","HP:0000938|Osteopenia|","HP:0000939|Osteoporosis|","HP:0000940|Abnormal diaphysis morphology|","HP:0001251|Ataxia|","HP:0001257|Spasticity|","HP:0001263|Global developmental delay|","HP:0001290|Generalized hypotonia|","HP:0001293|Cranial nerve compression|","HP:0001298|Encephalopathy|","HP:0001324|Muscle weakness|","HP:0001376|Limitation of joint mobility|","HP:0001392|Abnormality of the liver|","HP:0001394|Cirrhosis|","HP:0001433|Hepatosplenomegaly|","HP:0001508|Failure to thrive|","HP:0001533|Slender build|","HP:0001639|Hypertrophic cardiomyopathy|","HP:0001648|Cor pulmonale|","HP:0001733|Pancreatitis|","HP:0001738|Exocrine pancreatic insufficiency|","HP:0001744|Splenomegaly|","HP:0001763|Pes planus|","HP:0001882|Decreased total leukocyte count|","HP:0001894|Thrombocytosis|","HP:0001903|Anemia|","HP:0001931|Hypochromic anemia|","HP:0001944|Dehydration|","HP:0001974|Increased total leukocyte count|","HP:0001999|Abnormal facial shape|","HP:0002007|Frontal bossing|","HP:0002014|Diarrhea|","HP:0002020|Gastroesophageal reflux|","HP:0002024|Malabsorption|","HP:0002035|Rectal prolapse|","HP:0002039|Anorexia|","HP:0002059|Cerebral atrophy|","HP:0002079|Hypoplasia of the corpus callosum|","HP:0002099|Asthma|","HP:0002105|Hemoptysis|","HP:0002107|Pneumothorax|","HP:0002110|Bronchiectasis|","HP:0002150|Hypercalciuria|","HP:0002167|Abnormal speech pattern|","HP:0002188|Delayed CNS myelination|","HP:0002205|Recurrent respiratory infections|","HP:0002240|Hepatomegaly|","HP:0002315|Headache|","HP:0002384|Focal impaired awareness seizure|","HP:0002515|Waddling gait|","HP:0002521|Hypsarrhythmia|","HP:0002570|Steatorrhea|","HP:0002595|Ileus|","HP:0002613|Biliary cirrhosis|","HP:0002644|Abnormal pelvic girdle bone morphology|","HP:0002650|Scoliosis|","HP:0002652|Skeletal dysplasia|","HP:0002653|Bone pain|","HP:0002673|Coxa valga|","HP:0002694|Sclerosis of skull base|","HP:0002724|Recurrent Aspergillus infections|","HP:0002726|Recurrent Staphylococcus aureus infections|","HP:0002783|Recurrent lower respiratory tract infections|","HP:0002808|Kyphosis|","HP:0002818|Abnormal morphology of the radius|","HP:0002823|Abnormal femur morphology|","HP:0002842|Recurrent Burkholderia cepacia infections|","HP:0002857|Genu valgum|","HP:0002910|Elevated circulating hepatic transaminase concentration|","HP:0002992|Abnormal tibia morphology|","HP:0003034|Diaphyseal sclerosis|","HP:0003202|Skeletal muscle atrophy|","HP:0003212|Increased circulating IgE concentration|","HP:0003237|Increased circulating IgG concentration|","HP:0003251|Male infertility|","HP:0003307|Hyperlordosis|","HP:0003388|Easy fatigability|","HP:0003565|Elevated erythrocyte sedimentation rate|","HP:0003593|Infantile onset|","HP:0003621|Juvenile onset|","HP:0003758|Reduced subcutaneous adipose tissue|"]}]}