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: C0155017
Disease: Color Blindness, Blue
Color Blindness, Blue 		0 12 0 0 1 9.6E-03
CUI: C0553573
Disease: Primary infertility
Primary infertility 		0 2 0 0 1 1.1E-02
CUI: C0860602
Disease: Anxious personality
Anxious personality 		0 2 0 0 1 1.1E-02
CUI: C1833450
Disease: HASHIMOTO THYROIDITIS, SUSCEPTIBILITY TO
HASHIMOTO THYROIDITIS, SUSCEPTIBILITY TO 		0 1 0 0 1 1.1E-02
CUI: C1857845
Disease: CELIAC DISEASE, SUSCEPTIBILITY TO, 3 (finding)
CELIAC DISEASE, SUSCEPTIBILITY TO, 3 (finding) 		0 1 0 0 1 1.1E-02
CUI: C0266435
Disease: Congenital hypoplasia of penis
Congenital hypoplasia of penis 		237 0 1 1.7E-03 0 0
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies 		219 0 1 1.8E-03 0 0
CUI: C0423109
Disease: Upward slant of palpebral fissure
Upward slant of palpebral fissure 		216 0 1 1.8E-03 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation 		215 0 1 1.8E-03 0 0
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		210 0 1 1.8E-03 0 0
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy 		194 0 1 1.9E-03 0 0
CUI: C1861324
Disease: Short philtrum
Short philtrum 		182 0 1 1.9E-03 0 0
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		163 0 1 2.0E-03 0 0
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding) 		160 0 1 2.0E-03 0 0
CUI: C0221358
Disease: Long narrow head
Long narrow head 		154 0 1 2.0E-03 0 0
CUI: C1857679
Disease: Sloping forehead
Sloping forehead 		149 0 1 2.1E-03 0 0
CUI: C0024433
Disease: Macrostomia
Macrostomia 		148 0 1 2.1E-03 0 0
CUI: C1839739
Disease: Thick lower lip vermilion
Thick lower lip vermilion 		145 0 1 2.1E-03 0 0
CUI: C0020490
Disease: Hyperopia
Hyperopia 		142 0 1 2.1E-03 0 0
CUI: C0152423
Disease: Congenital small ears
Congenital small ears 		137 0 1 2.1E-03 0 0
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator 		131 0 1 2.1E-03 0 0
CUI: C0009363
Disease: Congenital ocular coloboma (disorder)
Congenital ocular coloboma (disorder) 		129 0 1 2.2E-03 0 0
CUI: C0079924
Disease: Oligohydramnios
Oligohydramnios 		129 0 1 2.2E-03 0 0
CUI: C0241355
Disease: Small testicle
Small testicle 		129 0 1 2.2E-03 0 0
CUI: C0234162
Disease: Cerebellar Dysmetria
Cerebellar Dysmetria 		127 0 1 2.2E-03 0 0