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| patient_id,phenotypes,degrees,attention | |
| UDN-P2,Abnormality of vision,111,0.1183807775378227 | |
| UDN-P2,Global developmental delay,1330,0.1499209105968475 | |
| UDN-P2,Abnormality of the liver,65,0.0950504913926124 | |
| UDN-P2,Failure to thrive in infancy,1,0.1553362309932708 | |
| UDN-P2,Exocrine pancreatic insufficiency,4,0.0865935012698173 | |
| UDN-P2,Abdominal pain,257,0.068713754415512 | |
| UDN-P2,Asthma,177,0.0740201994776725 | |
| UDN-P2,Duodenal atresia,34,0.064612977206707 | |
| UDN-P2,Intestinal malrotation,91,0.0643364712595939 | |
| UDN-P2,Gastroparesis,23,0.1230346783995628 | |
| UDN-P1,Thick lower lip vermilion,1,0.0236996822059154 | |
| UDN-P1,Hydrocephalus,304,0.0230413302779197 | |
| UDN-P1,Microcephaly,1006,0.0316418893635273 | |
| UDN-P1,Low anterior hairline,4,0.0270521882921457 | |
| UDN-P1,Mandibular prognathia,6,0.026597810909152 | |
| UDN-P1,Alacrima,1,0.0138036329299211 | |
| UDN-P1,Thick eyebrow,8,0.0170831736177206 | |
| UDN-P1,Exotropia,94,0.0167111363261938 | |
| UDN-P1,Synophrys,3,0.0241384990513324 | |
| UDN-P1,Delayed eruption of teeth,131,0.0224792174994945 | |
| UDN-P1,Abnormal sternum morphology,51,0.0120808342471718 | |
| UDN-P1,Hypertension,278,0.0193403456360101 | |
| UDN-P1,Hypotonia,911,0.0355296544730663 | |
| UDN-P1,Global developmental delay,1330,0.0301800202578306 | |
| UDN-P1,Dystonia,360,0.0236831586807966 | |
| UDN-P1,Absent speech,1,0.0214502979069948 | |
| UDN-P1,Failure to thrive,648,0.0351606905460357 | |
| UDN-P1,Growth delay,435,0.0286059584468603 | |
| UDN-P1,Pancreatitis,63,0.0134885320439934 | |
| UDN-P1,Overlapping toe,2,0.0212031248956918 | |
| UDN-P1,Constipation,270,0.0162120759487152 | |
| UDN-P1,Gastroesophageal reflux,268,0.0238284692168235 | |
| UDN-P1,Cerebral atrophy,231,0.0270951297134161 | |
| UDN-P1,Hypoplasia of the corpus callosum,332,0.0298781190067529 | |
| UDN-P1,Respiratory insufficiency,325,0.0320345684885978 | |
| UDN-P1,Ventriculomegaly,409,0.0279995389282703 | |
| UDN-P1,Coarse hair,2,0.032378576695919 | |
| UDN-P1,Drooling,85,0.0170378927141428 | |
| UDN-P1,Febrile seizure (within the age range of 3 months to 6 years),62,0.0118239596486091 | |
| UDN-P1,Developmental regression,203,0.0243585351854562 | |
| UDN-P1,Abnormal cerebral white matter morphology,76,0.0176227763295173 | |
| UDN-P1,Short stature,1167,0.0382893718779087 | |
| UDN-P1,Chronic pancreatitis,1,0.0170067008584737 | |
| UDN-P1,Premature loss of primary teeth,1,0.0167370326817035 | |
| UDN-P1,Premature loss of teeth,32,0.0260231960564851 | |
| UDN-P1,Chronic lung disease,1,0.0176592171192169 | |
| UDN-P1,Moderate sensorineural hearing impairment,1,0.009951589629054 | |
| UDN-P1,Laryngeal cleft,1,0.0077759157866239 | |
| UDN-P1,Laryngeal calcification,1,0.0125970430672168 | |
| UDN-P1,Low hanging columella,2,0.0163100585341453 | |
| UDN-P1,Prominent eyelashes,1,0.024880614131689 | |
| UDN-P1,Gastrostomy tube feeding in infancy,1,0.0276554562151432 | |
| UDN-P1,Midface retrusion,1,0.0258742850273847 | |
| UDN-P1,Premature adrenarche,1,0.0266624484211206 | |
| UDN-P1,T2 hypointense brainstem,1,0.0004453512665349 | |
| UDN-P1,T2 hypointense basal ganglia,49,0.0048909387551248 | |