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: C4025886
Disease: Severe periodontitis
Severe periodontitis 		0 12 0 0 2 2.3E-02
CUI: C0220743
Disease: Childhood hypophosphatasia (disorder)
Childhood hypophosphatasia (disorder) 		1 17 1 8.3E-02 13 0.16
CUI: C0849668
Disease: peri-menopausal
peri-menopausal 		1 0 1 8.3E-02 0 0
CUI: C1744705
Disease: Atrophy of optic disc
Atrophy of optic disc 		1 0 1 8.3E-02 0 0
CUI: C1840322
Disease: ODONTOHYPOPHOSPHATASIA (disorder)
ODONTOHYPOPHOSPHATASIA (disorder) 		1 4 1 8.3E-02 1 1.3E-02
CUI: C1845407
Disease: CONE-ROD DYSTROPHY, X-LINKED, 3
CONE-ROD DYSTROPHY, X-LINKED, 3 		1 0 1 8.3E-02 0 0
CUI: C1855815
Disease: Skin dimple over apex of long bone angulation
Skin dimple over apex of long bone angulation 		1 0 1 8.3E-02 0 0
CUI: C2673477
Disease: Hypophosphatasia, Perinatal Lethal
Hypophosphatasia, Perinatal Lethal 		1 2 1 8.3E-02 2 2.6E-02
CUI: C3825592
Disease: Thromboembolism in children
Thromboembolism in children 		1 0 1 8.3E-02 0 0
CUI: C4016457
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A, SEVERE
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A, SEVERE 		1 0 1 8.3E-02 0 0
CUI: C4023157
Disease: Elevated plasma pyrophosphate
Elevated plasma pyrophosphate 		1 0 1 8.3E-02 0 0
CUI: C4025607
Disease: Elevated urine pyrophosphate
Elevated urine pyrophosphate 		1 0 1 8.3E-02 0 0
CUI: C4072995
Disease: Difficulty adjusting from light to dark
Difficulty adjusting from light to dark 		1 0 1 8.3E-02 0 0
CUI: C4693933
Disease: HYPEREKPLEXIA 4
HYPEREKPLEXIA 4 		1 0 1 8.3E-02 0 0
CUI: C1827996
Disease: Ovarian cancer, disseminated
Ovarian cancer, disseminated 		2 0 1 7.7E-02 0 0
CUI: C1855828
Disease: Vertebral clefting
Vertebral clefting 		2 0 1 7.7E-02 0 0
CUI: C1857618
Disease: Achromatopsia 2
Achromatopsia 2 		2 0 1 7.7E-02 0 0
CUI: C1860202
Disease: Unossified vertebral bodies
Unossified vertebral bodies 		2 0 1 7.7E-02 0 0
CUI: C1879279
Disease: adult nasal type extranodal NK/T-cell lymphoma
adult nasal type extranodal NK/T-cell lymphoma 		2 0 1 7.7E-02 0 0
CUI: C1879280
Disease: childhood nasal type extranodal NK/T-cell lymphoma
childhood nasal type extranodal NK/T-cell lymphoma 		2 0 1 7.7E-02 0 0
CUI: C0409860
Disease: Rotator cuff tear arthropathy
Rotator cuff tear arthropathy 		3 0 1 7.1E-02 0 0
CUI: C1858806
Disease: CONE-ROD DYSTROPHY 3 (disorder)
CONE-ROD DYSTROPHY 3 (disorder) 		3 0 1 7.1E-02 0 0
CUI: C1969738
Disease: Premature loss of permanent teeth
Premature loss of permanent teeth 		3 0 1 7.1E-02 0 0
CUI: C2919327
Disease: Pleomorphic lobular carcinoma in situ
Pleomorphic lobular carcinoma in situ 		3 0 1 7.1E-02 0 0
CUI: C4073107
Disease: Incomplete congenital stationary night blindness
Incomplete congenital stationary night blindness 		3 0 1 7.1E-02 0 0