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| patient_id,phenotypes,degrees,attention | |
| UDN-P2,Abnormality of vision,111,0.0989853367209434 | |
| UDN-P2,Global developmental delay,1330,0.1393505930900573 | |
| UDN-P2,Abnormality of the liver,65,0.0837447270750999 | |
| UDN-P2,Failure to thrive in infancy,1,0.1541623473167419 | |
| UDN-P2,Exocrine pancreatic insufficiency,4,0.0962460488080978 | |
| UDN-P2,Abdominal pain,257,0.0696877762675285 | |
| UDN-P2,Asthma,177,0.0721269026398658 | |
| UDN-P2,Duodenal atresia,34,0.0989027693867683 | |
| UDN-P2,Intestinal malrotation,91,0.0801789388060569 | |
| UDN-P2,Gastroparesis,23,0.106614664196968 | |
| UDN-P9,Flat glenoid fossa,1,0.0665825009346008 | |
| UDN-P9,Abnormality of the vertebral column,76,0.0361983776092529 | |
| UDN-P9,Platyspondyly,129,0.0615288130939006 | |
| UDN-P9,Cutis marmorata,62,0.0318356454372406 | |
| UDN-P9,Wormian bones,1,0.0537327453494071 | |
| UDN-P9,Scoliosis,801,0.0558811277151107 | |
| UDN-P9,Spondylometaphyseal dysplasia,9,0.0940656214952468 | |
| UDN-P9,Coxa vara,56,0.0579654388129711 | |
| UDN-P9,Abnormality of the lower limb,48,0.0458225421607494 | |
| UDN-P9,Thoracic scoliosis,30,0.0464530810713768 | |
| UDN-P9,Genu varum,57,0.073094867169857 | |
| UDN-P9,Tibial bowing,43,0.0525600053369998 | |
| UDN-P9,Abnormal form of the vertebral bodies,138,0.0546819157898426 | |
| UDN-P9,Short stature,1167,0.0585363544523716 | |
| UDN-P9,Abnormality of the femoral metaphysis,10,0.0352263785898685 | |
| UDN-P9,Abnormality of femoral epiphysis,10,0.0409332402050495 | |
| UDN-P9,Abnormality of lower limb epiphysis morphology,6,0.0124136246740818 | |
| UDN-P9,Acetabular dysplasia,1,0.0529508516192436 | |
| UDN-P9,Short femoral neck,1,0.0695368871092796 | |
| UDN-P7,Elevated serum creatine kinase,219,0.156127393245697 | |
| UDN-P7,Generalized muscle weakness,1,0.139058843255043 | |
| UDN-P7,Muscular dystrophy,52,0.1362844258546829 | |
| UDN-P7,Proximal muscle weakness,120,0.1536363512277603 | |
| UDN-P7,Calf muscle pseudohypertrophy,1,0.1570710241794586 | |
| UDN-P7,Abnormal muscle fiber morphology,39,0.0849768370389938 | |
| UDN-P7,Toe walking,1,0.1728451550006866 | |
| UDN-P8,Muscle weakness,392,0.0540948249399662 | |
| UDN-P8,Hypertrophic cardiomyopathy,153,0.0568107031285762 | |
| UDN-P8,Cerebral atrophy,231,0.0622156262397766 | |
| UDN-P8,Hypoplasia of the corpus callosum,332,0.0678444355726242 | |
| UDN-P8,Limb hypertonia,47,0.0716666877269744 | |
| UDN-P8,Lactic acidosis,122,0.0437235236167907 | |
| UDN-P8,Abnormality of temperature regulation,23,0.0598855391144752 | |
| UDN-P8,Respiratory failure requiring assisted ventilation,31,0.0432068929076194 | |
| UDN-P8,Cerebral hypomyelination,19,0.0751257538795471 | |
| UDN-P8,Infantile axial hypotonia,2,0.0626801550388336 | |
| UDN-P8,EEG with focal slow activity,4,0.0187200624495744 | |
| UDN-P8,EEG with generalized slow activity,13,0.0373874828219413 | |
| UDN-P8,Infantile spasms,3,0.0651202574372291 | |
| UDN-P8,Elevated brain lactate level by MRS,4,0.0452156253159046 | |
| UDN-P8,Profound global developmental delay,1,0.0835469588637352 | |
| UDN-P8,Abnormal cerebral morphology,25,0.0396268218755722 | |
| UDN-P8,Cerebral visual impairment,97,0.0617175139486789 | |
| UDN-P8,Oral-pharyngeal dysphagia,1,0.0514112450182437 | |