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: C1410927
Disease: Narrow angle
Narrow angle 		3 0 3 0.11 0 0
CUI: C1302995
Disease: Congenital Fibrosis of the Extraocular Muscles
Congenital Fibrosis of the Extraocular Muscles 		13 4 3 7.9E-02 1 0.20
CUI: C1838625
Disease: Warburg Sjo Fledelius syndrome
Warburg Sjo Fledelius syndrome 		16 0 3 7.3E-02 0 0
CUI: C3494623
Disease: Mild dementia
Mild dementia 		16 0 3 7.3E-02 0 0
CUI: C0266521
Disease: Marcus Gunn phenomenon
Marcus Gunn phenomenon 		2 0 2 7.1E-02 0 0
CUI: C0432066
Disease: Congenital malformation syndromes affecting facial appearance
Congenital malformation syndromes affecting facial appearance 		2 0 2 7.1E-02 0 0
CUI: C0853240
Disease: Mobius II syndrome
Mobius II syndrome 		2 0 2 7.1E-02 0 0
CUI: C1836217
Disease: Tukel syndrome
Tukel syndrome 		2 0 2 7.1E-02 0 0
CUI: C1846911
Disease: Compensatory chin elevation
Compensatory chin elevation 		2 0 2 7.1E-02 0 0
CUI: C1851107
Disease: Levator palpebrae superioris atrophy
Levator palpebrae superioris atrophy 		2 0 2 7.1E-02 0 0
CUI: C1851108
Disease: Superior rectus atrophy
Superior rectus atrophy 		2 0 2 7.1E-02 0 0
CUI: C2750404
Disease: Fibrosis of Extraocular Muscles, Congenital, 3C
Fibrosis of Extraocular Muscles, Congenital, 3C 		2 0 2 7.1E-02 0 0
CUI: C2751105
Disease: FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3B (disorder)
FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3B (disorder) 		2 0 2 7.1E-02 0 0
CUI: C0687154
Disease: Acrocephalopolysyndactyly
Acrocephalopolysyndactyly 		3 0 2 6.9E-02 0 0
CUI: C1865915
Disease: FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 2
FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 2 		3 0 2 6.9E-02 0 0
CUI: C2748801
Disease: FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3A, WITH OR WITHOUT EXTRAOCULAR INVOLVEMENT
FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3A, WITH OR WITHOUT EXTRAOCULAR INVOLVEMENT 		3 9 2 6.9E-02 1 1.0E-01
CUI: C3898473
Disease: Malignant biliary obstruction
Malignant biliary obstruction 		3 0 2 6.9E-02 0 0
CUI: C4015552
Disease: FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 5
FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 5 		3 0 2 6.9E-02 0 0
CUI: C0001193
Disease: Apert syndrome
Apert syndrome 		20 0 3 6.7E-02 0 0
CUI: C1851102
Disease: Fibrosis Of Extraocular Muscles, Congenital, 1
Fibrosis Of Extraocular Muscles, Congenital, 1 		4 0 2 6.7E-02 0 0
CUI: C0265240
Disease: Goldenhar Syndrome
Goldenhar Syndrome 		21 0 3 6.5E-02 0 0
CUI: C4024213
Disease: Aplasia of the pectoralis major muscle
Aplasia of the pectoralis major muscle 		5 0 2 6.5E-02 0 0
CUI: C0242006
Disease: Myelofibrosis due to another disorder
Myelofibrosis due to another disorder 		23 0 3 6.2E-02 0 0
CUI: C1318541
Disease: Sertoli-Leydig cell tumor of intermediate differentiation
Sertoli-Leydig cell tumor of intermediate differentiation 		6 0 2 6.2E-02 0 0
CUI: C1833219
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B (disorder)
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B (disorder) 		6 0 2 6.2E-02 0 0