Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0746674
Disease: Generalized muscle weakness
Generalized muscle weakness 		126 0 1 2.6E-03 0 0
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		124 0 1 2.7E-03 0 0
CUI: C0014877
Disease: Esotropia
Esotropia 		121 0 1 2.7E-03 0 0
CUI: C0427065
Disease: Distal muscle weakness
Distal muscle weakness 		117 0 1 2.7E-03 0 0
CUI: C4552811
Disease: Generalized Muscle Weakness, CTCAE
Generalized Muscle Weakness, CTCAE 		117 0 1 2.7E-03 0 0
CUI: C0231712
Disease: Waddling gait
Waddling gait 		113 0 1 2.7E-03 0 0
CUI: C1848736
Disease: Distal amyotrophy
Distal amyotrophy 		106 0 1 2.8E-03 0 0
CUI: C4551493
Disease: Situs inversus totalis
Situs inversus totalis 		104 0 1 2.8E-03 0 0
CUI: C1837142
Disease: Poor suck
Poor suck 		103 0 1 2.8E-03 0 0
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement 		96 0 1 2.9E-03 0 0
CUI: C0013132
Disease: Drooling
Drooling 		95 0 1 2.9E-03 0 0
CUI: C1836543
Disease: Thick vermilion border
Thick vermilion border 		95 0 1 2.9E-03 0 0
CUI: C0009398
Disease: Color vision defect
Color vision defect 		94 0 1 2.9E-03 0 0
CUI: C0014548
Disease: Epilepsy, Generalized
Epilepsy, Generalized 		93 0 1 2.9E-03 0 0
CUI: C0566620
Disease: Nasal voice
Nasal voice 		93 0 1 2.9E-03 0 0
CUI: C0729353
Disease: Subfertility
Subfertility 		91 0 1 2.9E-03 0 0
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure 		88 0 1 2.9E-03 0 0
CUI: C0086237
Disease: Epilepsy, Cryptogenic
Epilepsy, Cryptogenic 		88 0 1 2.9E-03 0 0
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index 		88 0 1 2.9E-03 0 0
CUI: C0085648
Disease: Synovial Cyst
Synovial Cyst 		87 0 1 2.9E-03 0 0
CUI: C0003537
Disease: Aphasia
Aphasia 		86 0 1 3.0E-03 0 0
CUI: C0878659
Disease: Disproportionate short stature
Disproportionate short stature 		86 0 1 3.0E-03 0 0
CUI: C4085590
Disease: Cone-Rod Dystrophies
Cone-Rod Dystrophies 		86 0 1 3.0E-03 0 0
CUI: C0002418
Disease: Amblyopia
Amblyopia 		85 0 1 3.0E-03 0 0
CUI: C0339525
Disease: Autosomal dominant retinitis pigmentosa
Autosomal dominant retinitis pigmentosa 		85 0 1 3.0E-03 0 0