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: C0037188
Disease: Sinoatrial Block
Sinoatrial Block 		1 0 1 2.6E-02 0 0
CUI: C0264356
Disease: Childhood bronchiectasis
Childhood bronchiectasis 		1 0 1 2.6E-02 0 0
CUI: C0264421
Disease: Occupational lung disease
Occupational lung disease 		1 0 1 2.6E-02 0 0
CUI: C0265201
Disease: De Sanctis-Cacchione syndrome
De Sanctis-Cacchione syndrome 		1 0 1 2.6E-02 0 0
CUI: C0266024
Disease: Moon's molar teeth
Moon's molar teeth 		1 0 1 2.6E-02 0 0
CUI: C0270910
Disease: Idiopathic peripheral neuropathy
Idiopathic peripheral neuropathy 		1 0 1 2.6E-02 0 0
CUI: C0277331
Disease: Disease due to Acanthocephala
Disease due to Acanthocephala 		1 0 1 2.6E-02 0 0
CUI: C0339434
Disease: Choroidal effusion
Choroidal effusion 		1 0 1 2.6E-02 0 0
CUI: C0344525
Disease: Congenital membranous cataract
Congenital membranous cataract 		1 0 1 2.6E-02 0 0
CUI: C0393697
Disease: Epilepsy with grand mal seizures on awakening (disorder)
Epilepsy with grand mal seizures on awakening (disorder) 		1 0 1 2.6E-02 0 0
CUI: C0403379
Disease: Emphysematous pyelonephritis
Emphysematous pyelonephritis 		1 0 1 2.6E-02 0 0
CUI: C0686709
Disease: Meningococcal conjunctivitis
Meningococcal conjunctivitis 		1 0 1 2.6E-02 0 0
CUI: C0751079
Disease: Diplopia, Vertical
Diplopia, Vertical 		1 0 1 2.6E-02 0 0
CUI: C0796031
Disease: Malouf syndrome
Malouf syndrome 		1 0 1 2.6E-02 0 0
CUI: C0796083
Disease: Najjar syndrome
Najjar syndrome 		1 0 1 2.6E-02 0 0
CUI: C1290646
Disease: Acute apical abscess
Acute apical abscess 		1 0 1 2.6E-02 0 0
CUI: C1300818
Disease: Necrotic tumor
Necrotic tumor 		1 0 1 2.6E-02 0 0
CUI: C1392110
Disease: Crystalline cataract
Crystalline cataract 		1 0 1 2.6E-02 0 0
CUI: C1833021
Disease: DEAFNESS, AUTOSOMAL DOMINANT 6
DEAFNESS, AUTOSOMAL DOMINANT 6 		1 0 1 2.6E-02 0 0
CUI: C1833229
Disease: Cataract, Congenital Zonular, with Sutural Opacities
Cataract, Congenital Zonular, with Sutural Opacities 		1 0 1 2.6E-02 0 0
CUI: C1835380
Disease: Labial pseudohypertrophy
Labial pseudohypertrophy 		1 0 1 2.6E-02 0 0
CUI: C1835389
Disease: Increased intramuscular fat
Increased intramuscular fat 		1 0 1 2.6E-02 0 0
CUI: C1837023
Disease: CATARACT, CONGENITAL, CERULEAN TYPE, 3
CATARACT, CONGENITAL, CERULEAN TYPE, 3 		1 0 1 2.6E-02 0 0
CUI: C1837317
Disease: Alpha-B Crystallinopathy
Alpha-B Crystallinopathy 		1 0 1 2.6E-02 0 0
CUI: C1850039
Disease: Pericardial Effusion, Chronic
Pericardial Effusion, Chronic 		1 0 1 2.6E-02 0 0