{"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:4177,10,HGNC:4177,165,0]["},"schema":"id|name|definition","mappings":[{"input":"HGNC:4177","source":"HGNC:4177|glucosylceramidase beta 1","targets":["HP:0000006|Autosomal dominant inheritance|","HP:0000007|Autosomal recessive inheritance|","HP:0000012|Urinary urgency|","HP:0000027|Azoospermia|","HP:0000093|Proteinuria|","HP:0000160|Narrow mouth|","HP:0000164|Abnormality of the dentition|","HP:0000194|Open mouth|","HP:0000211|Trismus|","HP:0000218|High palate|","HP:0000225|Gingival bleeding|","HP:0000232|Everted lower lip vermilion|","HP:0000238|Hydrocephalus|","HP:0000248|Brachycephaly|","HP:0000252|Microcephaly|","HP:0000278|Retrognathia|","HP:0000298|Mask-like facies|","HP:0000316|Hypertelorism|","HP:0000325|Triangular face|","HP:0000338|Hypomimic face|","HP:0000347|Micrognathia|","HP:0000358|Posteriorly rotated ears|","HP:0000369|Low-set ears|","HP:0000407|Sensorineural hearing impairment|","HP:0000421|Epistaxis|","HP:0000463|Anteverted nares|","HP:0000478|Abnormality of the eye|","HP:0000486|Strabismus|","HP:0000508|Ptosis|","HP:0000565|Esotropia|","HP:0000570|Abnormal saccadic eye movements|","HP:0000602|Ophthalmoplegia|","HP:0000605|Supranuclear gaze palsy|","HP:0000623|Supranuclear ophthalmoplegia|","HP:0000651|Diplopia|","HP:0000656|Ectropion|","HP:0000657|Oculomotor apraxia|","HP:0000666|Horizontal nystagmus|","HP:0000674|Anodontia|","HP:0000713|Agitation|","HP:0000716|Depression|","HP:0000726|Dementia|","HP:0000737|Irritability|","HP:0000738|Hallucinations|","HP:0000741|Apathy|","HP:0000744|Low frustration tolerance|","HP:0000746|Delusion|","HP:0000751|Personality changes|","HP:0000767|Pectus excavatum|","HP:0000790|Hematuria|","HP:0000822|Hypertension|","HP:0000823|Delayed puberty|","HP:0000938|Osteopenia|","HP:0000939|Osteoporosis|","HP:0000953|Hyperpigmentation of the skin|","HP:0000962|Hyperkeratosis|","HP:0000967|Petechiae|","HP:0000974|Hyperextensible skin|","HP:0000978|Bruising susceptibility|","HP:0000979|Purpura|","HP:0001081|Cholelithiasis|","HP:0001249|Intellectual disability|","HP:0001250|Seizure|","HP:0001251|Ataxia|","HP:0001252|Hypotonia|","HP:0001257|Spasticity|","HP:0001258|Spastic paraplegia|","HP:0001260|Dysarthria|","HP:0001263|Global developmental delay|","HP:0001265|Hyporeflexia|","HP:0001268|Mental deterioration|","HP:0001270|Motor delay|","HP:0001276|Hypertonia|","HP:0001288|Gait disturbance|","HP:0001298|Encephalopathy|","HP:0001300|Parkinsonism|","HP:0001332|Dystonia|","HP:0001336|Myoclonus|","HP:0001337|Tremor|","HP:0001347|Hyperreflexia|","HP:0001371|Flexion contracture|","HP:0001394|Cirrhosis|","HP:0001399|Hepatic failure|","HP:0001409|Portal hypertension|","HP:0001433|Hepatosplenomegaly|","HP:0001508|Failure to thrive|","HP:0001510|Growth delay|","HP:0001511|Intrauterine growth retardation|","HP:0001522|Death in infancy|","HP:0001538|Protuberant abdomen|","HP:0001541|Ascites|","HP:0001558|Decreased fetal movement|","HP:0001561|Polyhydramnios|","HP:0001621|Weak voice|","HP:0001622|Premature birth|","HP:0001637|Abnormal myocardium morphology|","HP:0001640|Cardiomegaly|","HP:0001650|Aortic valve stenosis|","HP:0001653|Mitral regurgitation|","HP:0001654|Abnormal heart valve morphology|"]}]}