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: C0028643
Disease: Numbness
Numbness 		0 2 0 0 1 1.1E-02
CUI: C0242453
Disease: Prostatism
Prostatism 		0 1 0 0 1 1.1E-02
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 1.0E-02
CUI: C0393907
Disease: Axonal sensorimotor neuropathy
Axonal sensorimotor neuropathy 		0 2 0 0 1 1.1E-02
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		168 0 1 2.5E-03 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal 		158 0 1 2.6E-03 0 0
CUI: C1857679
Disease: Sloping forehead
Sloping forehead 		149 0 1 2.6E-03 0 0
CUI: C0005938
Disease: Bone Density
Bone Density 		138 0 1 2.7E-03 0 0
CUI: C0018498
Disease: Hair Color
Hair Color 		130 0 1 2.8E-03 0 0
CUI: C0030232
Disease: Pallor
Pallor 		124 0 1 2.8E-03 0 0
CUI: C0162701
Disease: Polysomnography
Polysomnography 		119 0 1 2.8E-03 0 0
CUI: C0476254
Disease: Dyslexia
Dyslexia 		118 0 1 2.9E-03 0 0
CUI: C0085631
Disease: Agitation
Agitation 		109 0 1 2.9E-03 0 0
CUI: C0266362
Disease: Ambiguous Genitalia
Ambiguous Genitalia 		109 0 1 2.9E-03 0 0
CUI: C0040264
Disease: Tinnitus
Tinnitus 		103 0 1 3.0E-03 0 0
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		100 0 1 3.0E-03 0 0
CUI: C0023015
Disease: Language Disorders
Language Disorders 		94 0 1 3.1E-03 0 0
CUI: C0432474
Disease: Klinefelter's syndrome - male with more than two X chromosomes
Klinefelter's syndrome - male with more than two X chromosomes 		90 0 1 3.1E-03 0 0
CUI: C0009080
Disease: Clubbed Fingers
Clubbed Fingers 		88 0 1 3.1E-03 0 0
CUI: C1963060
Disease: Agitation, CTCAE 3.0
Agitation, CTCAE 3.0 		87 0 1 3.1E-03 0 0
CUI: C4552855
Disease: Agitation, CTCAE 5.0
Agitation, CTCAE 5.0 		87 0 1 3.1E-03 0 0
CUI: C0426970
Disease: Spastic Quadriplegia
Spastic Quadriplegia 		86 0 1 3.1E-03 0 0
CUI: C4085590
Disease: Cone-Rod Dystrophies
Cone-Rod Dystrophies 		86 0 1 3.1E-03 0 0
CUI: C4551570
Disease: 2-3 toe syndactyly
2-3 toe syndactyly 		85 0 1 3.2E-03 0 0
CUI: C0339527
Disease: Leber Congenital Amaurosis
Leber Congenital Amaurosis 		83 0 1 3.2E-03 0 0