{"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:3942,10,HGNC:3942,40,2]["},"schema":"id|name|definition","mappings":[{"input":"HGNC:3942","source":"HGNC:3942|mechanistic target of rapamycin kinase","targets":["HP:0000006|Autosomal dominant inheritance|","HP:0000028|Cryptorchidism|","HP:0000047|Hypospadias|","HP:0000154|Wide mouth|","HP:0000194|Open mouth|","HP:0000219|Thin upper lip vermilion|","HP:0000256|Macrocephaly|","HP:0000260|Wide anterior fontanel|","HP:0000267|Cranial asymmetry|","HP:0000316|Hypertelorism|","HP:0000319|Smooth philtrum|","HP:0000331|Short chin|","HP:0000343|Long philtrum|","HP:0000348|High forehead|","HP:0000486|Strabismus|","HP:0000494|Downslanted palpebral fissures|","HP:0000648|Optic atrophy|","HP:0000729|Autistic behavior|","HP:0000752|Hyperactivity|","HP:0000929|Abnormal skull morphology|","HP:0000957|Cafe-au-lait spot|","HP:0001028|Hemangioma|","HP:0001053|Hypopigmented skin patches|","HP:0001249|Intellectual disability|","HP:0001250|Seizure|","HP:0001252|Hypotonia|","HP:0001263|Global developmental delay|","HP:0001269|Hemiparesis|","HP:0001273|Abnormal corpus callosum morphology|","HP:0001288|Gait disturbance|","HP:0001290|Generalized hypotonia|","HP:0001302|Pachygyria|","HP:0001328|Specific learning disability|","HP:0001336|Myoclonus|","HP:0001355|Megalencephaly|","HP:0001442|Typified by somatic mosaicism|","HP:0001520|Large for gestational age|","HP:0001537|Umbilical hernia|","HP:0001538|Protuberant abdomen|","HP:0001540|Diastasis recti|","HP:0001763|Pes planus|","HP:0001869|Deep plantar creases|","HP:0001873|Thrombocytopenia|","HP:0001943|Hypoglycemia|","HP:0001998|Neonatal hypoglycemia|","HP:0001999|Abnormal facial shape|","HP:0002007|Frontal bossing|","HP:0002079|Hypoplasia of the corpus callosum|","HP:0002099|Asthma|","HP:0002119|Ventriculomegaly|","HP:0002126|Polymicrogyria|","HP:0002133|Status epilepticus|","HP:0002167|Abnormal speech pattern|","HP:0002171|Gliosis|","HP:0002197|Generalized-onset seizure|","HP:0002212|Curly hair|","HP:0002282|Gray matter heterotopia|","HP:0002384|Focal impaired awareness seizure|","HP:0002392|EEG with polyspike wave complexes|","HP:0002446|Astrocytosis|","HP:0002539|Cortical dysplasia|","HP:0002720|Decreased circulating IgA concentration|","HP:0003196|Short nose|","HP:0003581|Adult onset|","HP:0003593|Infantile onset|","HP:0003745|Sporadic|","HP:0004302|Functional motor deficit|","HP:0004789|Lactose intolerance|","HP:0005257|Thoracic hypoplasia|","HP:0005266|Intestinal polyp|","HP:0005280|Depressed nasal bridge|","HP:0006191|Deep palmar crease|","HP:0006824|Cranial nerve paralysis|","HP:0007042|Focal white matter lesions|","HP:0007206|Hemimegalencephaly|","HP:0007359|Focal-onset seizure|","HP:0008905|Rhizomelia|","HP:0009882|Short distal phalanx of finger|","HP:0010241|Short proximal phalanx of finger|","HP:0010819|Atonic seizure|","HP:0010851|EEG with burst suppression|","HP:0010864|Severe intellectual disability|","HP:0011097|Epileptic spasm|","HP:0011153|Focal motor seizure|","HP:0011167|Focal tonic seizure|","HP:0011193|EEG with focal spikes|","HP:0011195|EEG with focal sharp slow waves|","HP:0011215|Hemihypsarrhythmia|","HP:0011220|Prominent forehead|","HP:0011800|Midface retrusion|","HP:0011968|Feeding difficulties|","HP:0012246|Oculomotor nerve palsy|","HP:0012377|Hemianopia|","HP:0012393|Allergy|","HP:0012650|Perisylvian polymicrogyria|","HP:0012757|Abnormal neuron morphology|","HP:0025104|Capillary malformation|","HP:0025373|Interictal EEG abnormality|","HP:0030890|Hyperintensity of cerebral white matter on MRI|","HP:0032046|Focal cortical dysplasia|"]}]}