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: C0035243
Disease: Respiratory Tract Infections
Respiratory Tract Infections 		0 10 0 0 1 1.5E-02
CUI: C0085129
Disease: Bronchial Hyperreactivity
Bronchial Hyperreactivity 		0 18 0 0 1 1.3E-02
CUI: C0155877
Disease: Allergic asthma
Allergic asthma 		0 55 0 0 1 8.8E-03
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0 1019 0 0 1 9.3E-04
CUI: C1827849
Disease: IgE-mediated allergic asthma
IgE-mediated allergic asthma 		0 46 0 0 1 9.6E-03
CUI: C0265971
Disease: Acrokeratosis Verruciformis of Hopf
Acrokeratosis Verruciformis of Hopf 		1 0 1 2.7E-02 0 0
CUI: C0274869
Disease: Toxic effect of heavy metal
Toxic effect of heavy metal 		1 0 1 2.7E-02 0 0
CUI: C0473575
Disease: Acantholytic Dyskeratotic Epidermal Nevus
Acantholytic Dyskeratotic Epidermal Nevus 		1 0 1 2.7E-02 0 0
CUI: C0878565
Disease: Electrocardiogram J wave
Electrocardiogram J wave 		1 0 1 2.7E-02 0 0
CUI: C1852296
Disease: Darier Disease, Acral Hemorrhagic Type
Darier Disease, Acral Hemorrhagic Type 		1 0 1 2.7E-02 0 0
CUI: C1852297
Disease: Darier Disease, Segmental
Darier Disease, Segmental 		1 0 1 2.7E-02 0 0
CUI: C1852311
Disease: Subungual hyperkeratotic fragments
Subungual hyperkeratotic fragments 		1 0 1 2.7E-02 0 0
CUI: C2678478
Disease: Brugada Syndrome 3
Brugada Syndrome 3 		1 0 1 2.7E-02 0 0
CUI: C2751807
Disease: Emery-Dreifuss Muscular Dystrophy 4
Emery-Dreifuss Muscular Dystrophy 4 		1 0 1 2.7E-02 0 0
CUI: C3554343
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 17
MENTAL RETARDATION, AUTOSOMAL DOMINANT 17 		1 0 1 2.7E-02 0 0
CUI: C3683483
Disease: Autosomal Recessive Cerebellar Ataxia Type 1
Autosomal Recessive Cerebellar Ataxia Type 1 		1 0 1 2.7E-02 0 0
CUI: C4016806
Disease: LYMPHOMA, SOMATIC
LYMPHOMA, SOMATIC 		1 0 1 2.7E-02 0 0
CUI: C4016913
Disease: T-CELL IMMUNODEFICIENCY, RECURRENT INFECTIONS, AUTOIMMUNITY, AND CARDIAC MALFORMATIONS
T-CELL IMMUNODEFICIENCY, RECURRENT INFECTIONS, AUTOIMMUNITY, AND CARDIAC MALFORMATIONS 		1 0 1 2.7E-02 0 0
CUI: C4018858
Disease: J wave
J wave 		1 0 1 2.7E-02 0 0
CUI: C4024899
Disease: Atrophy/Degeneration affecting the central nervous system
Atrophy/Degeneration affecting the central nervous system 		1 0 1 2.7E-02 0 0
CUI: C4509113
Disease: bipolar type I disorder
bipolar type I disorder 		1 0 1 2.7E-02 0 0
CUI: C4707155
Disease: Autosomal recessive myogenic arthrogryposis multiplex congenita
Autosomal recessive myogenic arthrogryposis multiplex congenita 		1 0 1 2.7E-02 0 0
CUI: C0238056
Disease: Chorea, Senile
Chorea, Senile 		2 0 1 2.6E-02 0 0
CUI: C0699728
Disease: Chronic progressive chorea
Chronic progressive chorea 		2 0 1 2.6E-02 0 0
CUI: C0854440
Disease: Fatty acid deficiency
Fatty acid deficiency 		2 0 1 2.6E-02 0 0