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: C0013575
Disease: Ectodermal Dysplasia
Ectodermal Dysplasia 		71 0 7 8.4E-02 0 0
CUI: C1845274
Disease: Abnormal conjugate eye movement
Abnormal conjugate eye movement 		7 5 2 8.3E-02 2 0.20
CUI: C4022735
Disease: Cerebral white matter atrophy
Cerebral white matter atrophy 		20 11 3 8.3E-02 2 0.12
CUI: C4022755
Disease: Functional abnormality of the gastrointestinal tract
Functional abnormality of the gastrointestinal tract 		7 0 2 8.3E-02 0 0
CUI: C1832348
Disease: Slow-growing hair
Slow-growing hair 		35 0 4 8.0E-02 0 0
CUI: C1845155
Disease: Exercise-induced myoglobinuria
Exercise-induced myoglobinuria 		8 2 2 8.0E-02 2 0.29
CUI: C1859347
Disease: Abnormal subcutaneous fat tissue distribution
Abnormal subcutaneous fat tissue distribution 		9 2 2 7.7E-02 2 0.29
CUI: C0264169
Disease: Saddle nose
Saddle nose 		10 0 2 7.4E-02 0 0
CUI: C1846006
Disease: Ectodermal dysplasia, hypohidrotic, with immune deficiency
Ectodermal dysplasia, hypohidrotic, with immune deficiency 		10 0 2 7.4E-02 0 0
CUI: C4072908
Disease: Induced vaginal delivery
Induced vaginal delivery 		10 10 2 7.4E-02 1 6.2E-02
CUI: C3539920
Disease: ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE
ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE 		25 0 3 7.3E-02 0 0
CUI: C3887494
Disease: ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE
ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE 		25 0 3 7.3E-02 0 0
CUI: C0041409
Disease: Turner Syndrome, Male
Turner Syndrome, Male 		11 0 2 7.1E-02 0 0
CUI: C0522055
Disease: Electrocardiogram abnormal
Electrocardiogram abnormal 		11 54 2 7.1E-02 2 3.4E-02
CUI: C1527404
Disease: Female Pseudo-Turner Syndrome
Female Pseudo-Turner Syndrome 		11 0 2 7.1E-02 0 0
CUI: C1328931
Disease: Multiple lentigines
Multiple lentigines 		13 0 2 6.7E-02 0 0
CUI: C3551431
Disease: Sparse or absent eyelashes
Sparse or absent eyelashes 		13 0 2 6.7E-02 0 0
CUI: C0235357
Disease: Hypoplasia of teeth
Hypoplasia of teeth 		14 0 2 6.5E-02 0 0
CUI: C0852413
Disease: Abnormal muscle tone
Abnormal muscle tone 		14 7 2 6.5E-02 1 7.7E-02
CUI: C1856408
Disease: Infantile encephalopathy
Infantile encephalopathy 		14 9 2 6.5E-02 2 0.14
CUI: C4025662
Disease: Abnormality of the ulna
Abnormality of the ulna 		14 0 2 6.5E-02 0 0
CUI: C0549629
Disease: Abnormal delivery
Abnormal delivery 		32 37 3 6.2E-02 1 2.3E-02
CUI: C1096666
Disease: Thyroid cancer metastatic
Thyroid cancer metastatic 		15 0 2 6.2E-02 0 0
CUI: C0574769
Disease: Loss of scalp hair
Loss of scalp hair 		16 4 2 6.1E-02 1 1.0E-01
CUI: C0518656
Disease: Chronic fatigue
Chronic fatigue 		17 2 2 5.9E-02 2 0.29