SHEPHERD / gene_discovery_scores_attn.csv
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patient_id,phenotypes,degrees,attention
UDN-P2,Abnormality of vision,111,0.1178910732269287
UDN-P2,Global developmental delay,1330,0.1363666206598281
UDN-P2,Abnormality of the liver,65,0.0964500233530998
UDN-P2,Failure to thrive in infancy,1,0.1844952553510666
UDN-P2,Exocrine pancreatic insufficiency,4,0.0708952322602272
UDN-P2,Abdominal pain,257,0.0660589486360549
UDN-P2,Asthma,177,0.0678283423185348
UDN-P2,Duodenal atresia,34,0.0732858255505561
UDN-P2,Intestinal malrotation,91,0.0733114182949066
UDN-P2,Gastroparesis,23,0.1134173870086669
UDN-P1,Thick lower lip vermilion,1,0.0254656299948692
UDN-P1,Hydrocephalus,304,0.0226140450686216
UDN-P1,Microcephaly,1006,0.0317770205438137
UDN-P1,Low anterior hairline,4,0.0236586183309555
UDN-P1,Mandibular prognathia,6,0.0236049313098192
UDN-P1,Alacrima,1,0.0144500378519296
UDN-P1,Thick eyebrow,8,0.0233250595629215
UDN-P1,Exotropia,94,0.0174672622233629
UDN-P1,Synophrys,3,0.0241911858320236
UDN-P1,Delayed eruption of teeth,131,0.0234366580843925
UDN-P1,Abnormal sternum morphology,51,0.0120793534442782
UDN-P1,Hypertension,278,0.0188926625996828
UDN-P1,Hypotonia,911,0.03265380859375
UDN-P1,Global developmental delay,1330,0.027355071157217
UDN-P1,Dystonia,360,0.0240448117256164
UDN-P1,Absent speech,1,0.022760335355997
UDN-P1,Failure to thrive,648,0.0337891578674316
UDN-P1,Growth delay,435,0.0274257939308881
UDN-P1,Pancreatitis,63,0.0125568015500903
UDN-P1,Overlapping toe,2,0.0273327771574258
UDN-P1,Constipation,270,0.0161661840975284
UDN-P1,Gastroesophageal reflux,268,0.0214648023247718
UDN-P1,Cerebral atrophy,231,0.0250347331166267
UDN-P1,Hypoplasia of the corpus callosum,332,0.0269252881407737
UDN-P1,Respiratory insufficiency,325,0.0316686779260635
UDN-P1,Ventriculomegaly,409,0.0280382838100194
UDN-P1,Coarse hair,2,0.024032786488533
UDN-P1,Drooling,85,0.0192697960883378
UDN-P1,Febrile seizure (within the age range of 3 months to 6 years),62,0.0105393650010228
UDN-P1,Developmental regression,203,0.0249004419893026
UDN-P1,Abnormal cerebral white matter morphology,76,0.0189827494323253
UDN-P1,Short stature,1167,0.036681056022644
UDN-P1,Chronic pancreatitis,1,0.0087832231074571
UDN-P1,Premature loss of primary teeth,1,0.0137059595435857
UDN-P1,Premature loss of teeth,32,0.0200045183300972
UDN-P1,Chronic lung disease,1,0.030693894252181
UDN-P1,Moderate sensorineural hearing impairment,1,0.0128651773557066
UDN-P1,Laryngeal cleft,1,0.0062378644943237
UDN-P1,Laryngeal calcification,1,0.0187820736318826
UDN-P1,Low hanging columella,2,0.0193525701761245
UDN-P1,Prominent eyelashes,1,0.0317739509046077
UDN-P1,Gastrostomy tube feeding in infancy,1,0.0312498826533556
UDN-P1,Midface retrusion,1,0.0272352565079927
UDN-P1,Premature adrenarche,1,0.0155880162492394
UDN-P1,T2 hypointense brainstem,1,0.0003417030384298
UDN-P1,T2 hypointense basal ganglia,49,0.0108007565140724