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: C0431371
Disease: Absence of septum pellucidum
Absence of septum pellucidum 		84 0 1 2.1E-03 0 0
CUI: C0040433
Disease: Tooth Crowding
Tooth Crowding 		82 0 1 2.1E-03 0 0
CUI: C0600031
Disease: Congenital absence of spleen
Congenital absence of spleen 		80 0 1 2.1E-03 0 0
CUI: C1839767
Disease: Tented upper lip vermilion
Tented upper lip vermilion 		79 0 1 2.2E-03 0 0
CUI: C0424731
Disease: Single transverse palmar crease
Single transverse palmar crease 		78 0 1 2.2E-03 0 0
CUI: C0424551
Disease: Impaired exercise tolerance
Impaired exercise tolerance 		76 0 1 2.2E-03 0 0
CUI: C0856863
Disease: Broad-based gait
Broad-based gait 		75 0 1 2.2E-03 0 0
CUI: C1839630
Disease: Severe muscular hypotonia
Severe muscular hypotonia 		75 0 1 2.2E-03 0 0
CUI: C3554617
Disease: Adducted thumb
Adducted thumb 		74 0 1 2.2E-03 0 0
CUI: C0339789
Disease: Congenital deafness
Congenital deafness 		72 0 1 2.2E-03 0 0
CUI: C0426415
Disease: Large nose
Large nose 		70 0 1 2.2E-03 0 0
CUI: C0455829
Disease: Waist Circumference
Waist Circumference 		70 0 1 2.2E-03 0 0
CUI: C1866141
Disease: Foot dorsiflexor weakness
Foot dorsiflexor weakness 		70 0 1 2.2E-03 0 0
CUI: C4025819
Disease: Abnormality of the hypothalamus-pituitary axis
Abnormality of the hypothalamus-pituitary axis 		70 0 1 2.2E-03 0 0
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome 		67 0 1 2.2E-03 0 0
CUI: C1850456
Disease: Progressive microcephaly
Progressive microcephaly 		67 0 1 2.2E-03 0 0
CUI: C0376705
Disease: Viral Load result
Viral Load result 		65 0 1 2.2E-03 0 0
CUI: C0025037
Disease: Meckel Diverticulum
Meckel Diverticulum 		63 0 1 2.2E-03 0 0
CUI: C0270960
Disease: Congenital myopathy (disorder)
Congenital myopathy (disorder) 		63 0 1 2.2E-03 0 0
CUI: C1847514
Disease: Postnatal microcephaly
Postnatal microcephaly 		62 0 1 2.2E-03 0 0
CUI: C0009024
Disease: Clonus
Clonus 		60 0 1 2.2E-03 0 0
CUI: C0020438
Disease: Hypercalciuria
Hypercalciuria 		60 0 1 2.2E-03 0 0
CUI: C0263523
Disease: Micronychia (disorder)
Micronychia (disorder) 		60 0 1 2.2E-03 0 0
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders 		59 0 1 2.2E-03 0 0
CUI: C0232744
Disease: Decreased liver function
Decreased liver function 		59 0 1 2.2E-03 0 0