{"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:4827,10,HGNC:4827,38,2]["},"schema":"id|name|definition","mappings":[{"input":"HGNC:4827","source":"HGNC:4827|hemoglobin subunit beta","targets":["HP:0000006|Autosomal dominant inheritance|","HP:0000007|Autosomal recessive inheritance|","HP:0000083|Renal insufficiency|","HP:0000114|Proximal tubulopathy|","HP:0000135|Hypogonadism|","HP:0000164|Abnormality of the dentition|","HP:0000488|Retinopathy|","HP:0000582|Upslanted palpebral fissure|","HP:0000707|Abnormality of the nervous system|","HP:0000737|Irritability|","HP:0000790|Hematuria|","HP:0000819|Diabetes mellitus|","HP:0000821|Hypothyroidism|","HP:0000822|Hypertension|","HP:0000823|Delayed puberty|","HP:0000829|Hypoparathyroidism|","HP:0000846|Adrenal insufficiency|","HP:0000924|Abnormality of the skeletal system|","HP:0000938|Osteopenia|","HP:0000939|Osteoporosis|","HP:0000952|Jaundice|","HP:0000953|Hyperpigmentation of the skin|","HP:0000961|Cyanosis|","HP:0000980|Pallor|","HP:0001081|Cholelithiasis|","HP:0001297|Stroke|","HP:0001392|Abnormality of the liver|","HP:0001394|Cirrhosis|","HP:0001395|Hepatic fibrosis|","HP:0001402|Hepatocellular carcinoma|","HP:0001406|Intrahepatic cholestasis|","HP:0001410|Decreased liver function|","HP:0001433|Hepatosplenomegaly|","HP:0001510|Growth delay|","HP:0001511|Intrauterine growth retardation|","HP:0001531|Failure to thrive in infancy|","HP:0001622|Premature birth|","HP:0001626|Abnormality of the cardiovascular system|","HP:0001640|Cardiomegaly|","HP:0001644|Dilated cardiomyopathy|","HP:0001722|High-output congestive heart failure|","HP:0001743|Abnormality of the spleen|","HP:0001744|Splenomegaly|","HP:0001746|Asplenia|","HP:0001878|Hemolytic anemia|","HP:0001891|Iron deficiency anemia|","HP:0001894|Thrombocytosis|","HP:0001899|Increased hematocrit|","HP:0001900|Increased circulating hemoglobin concentration|","HP:0001901|Polycythemia|","HP:0001903|Anemia|","HP:0001923|Reticulocytosis|","HP:0001930|Nonspherocytic hemolytic anemia|","HP:0001931|Hypochromic anemia|","HP:0001935|Microcytic anemia|","HP:0001954|Recurrent fever|","HP:0001971|Hypersplenism|","HP:0001974|Increased total leukocyte count|","HP:0001978|Extramedullary hematopoiesis|","HP:0002007|Frontal bossing|","HP:0002014|Diarrhea|","HP:0002027|Abdominal pain|","HP:0002092|Pulmonary arterial hypertension|","HP:0002094|Dyspnea|","HP:0002113|Pulmonary infiltrates|","HP:0002140|Ischemic stroke|","HP:0002176|Spinal cord compression|","HP:0002240|Hepatomegaly|","HP:0002597|Abnormality of the vasculature|","HP:0002659|Increased susceptibility to fractures|","HP:0002718|Recurrent bacterial infections|","HP:0002719|Recurrent infections|","HP:0002721|Immunodeficiency|","HP:0002754|Osteomyelitis|","HP:0002829|Arthralgia|","HP:0002857|Genu valgum|","HP:0003259|Elevated circulating creatinine concentration|","HP:0003281|Increased circulating ferritin concentration|","HP:0003330|Abnormal bone structure|","HP:0004349|Reduced bone mineral density|","HP:0004817|Drug-sensitive hemolytic anemia|","HP:0004823|Anisopoikilocytosis|","HP:0004840|Hypochromic microcytic anemia|","HP:0004870|Chronic hemolytic anemia|","HP:0004936|Venous thrombosis|","HP:0005268|Miscarriage|","HP:0005280|Depressed nasal bridge|","HP:0005511|Heinz body anemia|","HP:0005518|Increased mean corpuscular volume|","HP:0005546|Increased red cell osmotic resistance|","HP:0005560|Imbalanced hemoglobin synthesis|","HP:0006487|Bowing of the long bones|","HP:0008282|Unconjugated hyperbilirubinemia|","HP:0008346|Increased red cell sickling tendency|","HP:0009004|Hypoplasia of the musculature|","HP:0010620|Malar prominence|","HP:0010885|Avascular necrosis|","HP:0010972|Anemia of inadequate production|","HP:0011031|Abnormality of iron homeostasis|","HP:0011273|Anisocytosis|"]}]}