{"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:795,10,HGNC:795,115,1]["},"schema":"id|name|definition","mappings":[{"input":"HGNC:795","source":"HGNC:795|ATM serine/threonine kinase","targets":["HP:0000006|Autosomal dominant inheritance|","HP:0000007|Autosomal recessive inheritance|","HP:0000035|Abnormal testis morphology|","HP:0000134|Female hypogonadism|","HP:0000147|Polycystic ovaries|","HP:0000246|Sinusitis|","HP:0000252|Microcephaly|","HP:0000486|Strabismus|","HP:0000496|Abnormality of eye movement|","HP:0000505|Visual impairment|","HP:0000524|Conjunctival telangiectasia|","HP:0000639|Nystagmus|","HP:0000708|Atypical behavior|","HP:0000716|Depression|","HP:0000737|Irritability|","HP:0000738|Hallucinations|","HP:0000739|Anxiety|","HP:0000750|Delayed speech and language development|","HP:0000778|Hypoplasia of the thymus|","HP:0000819|Diabetes mellitus|","HP:0000823|Delayed puberty|","HP:0000957|Cafe-au-lait spot|","HP:0001123|Visual field defect|","HP:0001250|Seizure|","HP:0001251|Ataxia|","HP:0001252|Hypotonia|","HP:0001257|Spasticity|","HP:0001260|Dysarthria|","HP:0001266|Choreoathetosis|","HP:0001276|Hypertonia|","HP:0001288|Gait disturbance|","HP:0001315|Reduced tendon reflexes|","HP:0001332|Dystonia|","HP:0001336|Myoclonus|","HP:0001337|Tremor|","HP:0001350|Slurred speech|","HP:0001371|Flexion contracture|","HP:0001402|Hepatocellular carcinoma|","HP:0001442|Typified by somatic mosaicism|","HP:0001508|Failure to thrive|","HP:0001595|Abnormal hair morphology|","HP:0001744|Splenomegaly|","HP:0001824|Weight loss|","HP:0001888|Decreased total lymphocyte count|","HP:0001909|Leukemia|","HP:0001945|Fever|","HP:0001952|Glucose intolerance|","HP:0002017|Nausea and vomiting|","HP:0002019|Constipation|","HP:0002024|Malabsorption|","HP:0002027|Abdominal pain|","HP:0002028|Chronic diarrhea|","HP:0002039|Anorexia|","HP:0002073|Progressive cerebellar ataxia|","HP:0002075|Dysdiadochokinesis|","HP:0002076|Migraine|","HP:0002080|Intention tremor|","HP:0002110|Bronchiectasis|","HP:0002167|Abnormal speech pattern|","HP:0002205|Recurrent respiratory infections|","HP:0002216|Premature graying of hair|","HP:0002239|Gastrointestinal hemorrhage|","HP:0002354|Memory impairment|","HP:0002376|Developmental regression|","HP:0002516|Increased intracranial pressure|","HP:0002540|Inability to walk|","HP:0002664|Neoplasm|","HP:0002665|Lymphoma|","HP:0002671|Basal cell carcinoma|","HP:0002715|Abnormality of the immune system|","HP:0002716|Lymphadenopathy|","HP:0002720|Decreased circulating IgA concentration|","HP:0002721|Immunodeficiency|","HP:0002783|Recurrent lower respiratory tract infections|","HP:0002837|Recurrent bronchitis|","HP:0002861|Melanoma|","HP:0002893|Pituitary adenoma|","HP:0002894|Neoplasm of the pancreas|","HP:0002910|Elevated circulating hepatic transaminase concentration|","HP:0003002|Breast carcinoma|","HP:0003006|Neuroblastoma|","HP:0003202|Skeletal muscle atrophy|","HP:0003220|Abnormality of chromosome stability|","HP:0003401|Paresthesia|","HP:0004313|Decreased circulating immunoglobulin concentration|","HP:0004315|Decreased circulating IgG concentration|","HP:0004322|Short stature|","HP:0004374|Hemiplegia/hemiparesis|","HP:0005357|Defective B cell differentiation|","HP:0005374|Cellular immunodeficiency|","HP:0005403|Decreased total T cell count|","HP:0005561|Abnormal bone marrow cell morphology|","HP:0005599|Hypopigmentation of hair|","HP:0005978|Type II diabetes mellitus|","HP:0006254|Elevated circulating alpha-fetoprotein concentration|","HP:0006721|Acute lymphoblastic leukemia|","HP:0006725|Pancreatic adenocarcinoma|","HP:0007018|Attention deficit hyperactivity disorder|","HP:0007256|Abnormal pyramidal sign|","HP:0007495|Prematurely aged appearance|"]}]}