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: C0242453
Disease: Prostatism
Prostatism 		0 1 0 0 1 2.9E-02
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 2.4E-02
CUI: C0751837
Disease: Gait Ataxia
Gait Ataxia 		172 0 1 2.2E-03 0 0
CUI: C1839739
Disease: Thick lower lip vermilion
Thick lower lip vermilion 		145 0 1 2.4E-03 0 0
CUI: C1136382
Disease: Sclerocystic Ovaries
Sclerocystic Ovaries 		144 0 1 2.4E-03 0 0
CUI: C0231686
Disease: Gait, Unsteady
Gait, Unsteady 		143 0 1 2.4E-03 0 0
CUI: C0018498
Disease: Hair Color
Hair Color 		130 0 1 2.4E-03 0 0
CUI: C1837397
Disease: Severe global developmental delay
Severe global developmental delay 		130 0 1 2.4E-03 0 0
CUI: C0266544
Disease: Microcornea
Microcornea 		129 0 1 2.5E-03 0 0
CUI: C1629609
Disease: Age at menopause
Age at menopause 		129 0 1 2.5E-03 0 0
CUI: C0010038
Disease: Corneal Opacity
Corneal Opacity 		113 0 1 2.6E-03 0 0
CUI: C1837770
Disease: Sparse hair
Sparse hair 		112 0 1 2.6E-03 0 0
CUI: C1835884
Disease: Triangular face
Triangular face 		111 0 1 2.6E-03 0 0
CUI: C1839758
Disease: Narrow forehead
Narrow forehead 		106 0 1 2.6E-03 0 0
CUI: C4021085
Disease: Abnormality of brain morphology
Abnormality of brain morphology 		104 0 1 2.6E-03 0 0
CUI: C0015644
Disease: Muscular fasciculation
Muscular fasciculation 		99 0 1 2.6E-03 0 0
CUI: C0578038
Disease: Thin lips
Thin lips 		99 0 1 2.6E-03 0 0
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement 		96 0 1 2.7E-03 0 0
CUI: C1836543
Disease: Thick vermilion border
Thick vermilion border 		95 0 1 2.7E-03 0 0
CUI: C3489733
Disease: Oculomotor apraxia
Oculomotor apraxia 		92 0 1 2.7E-03 0 0
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement 		90 0 1 2.7E-03 0 0
CUI: C0426970
Disease: Spastic Quadriplegia
Spastic Quadriplegia 		86 0 1 2.7E-03 0 0
CUI: C3806467
Disease: Respiratory insufficiency due to muscle weakness
Respiratory insufficiency due to muscle weakness 		85 0 1 2.7E-03 0 0
CUI: C0431371
Disease: Absence of septum pellucidum
Absence of septum pellucidum 		84 0 1 2.8E-03 0 0
CUI: C0339527
Disease: Leber Congenital Amaurosis
Leber Congenital Amaurosis 		83 0 1 2.8E-03 0 0