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: C1849193
Disease: PEELING SKIN SYNDROME
PEELING SKIN SYNDROME 		67 0 6 2.9E-02 0 0
CUI: C1842937
Disease: AURAL ATRESIA, CONGENITAL
AURAL ATRESIA, CONGENITAL 		110 0 7 2.8E-02 0 0
CUI: C0023343
Disease: Leprosy
Leprosy 		190 120 9 2.7E-02 1 1.5E-03
CUI: C0019100
Disease: Severe Dengue
Severe Dengue 		117 0 7 2.7E-02 0 0
CUI: C2103602
Disease: Autoimmune Primary Adrenal Insufficiency
Autoimmune Primary Adrenal Insufficiency 		41 0 5 2.7E-02 0 0
CUI: C3541994
Disease: Drug Hypersensitivity Syndrome
Drug Hypersensitivity Syndrome 		43 0 5 2.7E-02 0 0
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		197 1019 9 2.7E-02 9 5.9E-03
CUI: C1848296
Disease: DOSAGE-SENSITIVE SEX REVERSAL
DOSAGE-SENSITIVE SEX REVERSAL 		159 0 8 2.7E-02 0 0
CUI: C0271737
Disease: Addison's disease due to autoimmunity
Addison's disease due to autoimmunity 		44 0 5 2.7E-02 0 0
CUI: C0497169
Disease: hiv-infection/aids
hiv-infection/aids 		124 0 7 2.6E-02 0 0
CUI: C0271073
Disease: Eales disease
Eales disease 		9 0 4 2.6E-02 0 0
CUI: C1960272
Disease: Latent autoimmune diabetes mellitus in adult
Latent autoimmune diabetes mellitus in adult 		49 0 5 2.6E-02 0 0
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		1675 954 46 2.6E-02 45 3.1E-02
CUI: C2936858
Disease: Congenital adrenal hyperplasia due to 21 hydroxylase deficiency
Congenital adrenal hyperplasia due to 21 hydroxylase deficiency 		50 0 5 2.6E-02 0 0
CUI: C0019360
Disease: Herpes zoster disease
Herpes zoster disease 		51 0 5 2.6E-02 0 0
CUI: C1274700
Disease: Postmenopausal frontal fibrosing alopecia
Postmenopausal frontal fibrosing alopecia 		11 0 4 2.6E-02 0 0
CUI: C4255374
Disease: Frontal fibrosing alopecia
Frontal fibrosing alopecia 		11 0 4 2.6E-02 0 0
CUI: C0343804
Disease: Chronic Chagas' disease
Chronic Chagas' disease 		52 0 5 2.6E-02 0 0
CUI: C0027121
Disease: Myositis
Myositis 		254 0 10 2.5E-02 0 0
CUI: C0015773
Disease: Felty Syndrome
Felty Syndrome 		13 0 4 2.5E-02 0 0
CUI: C0268287
Disease: Deficiency of steroid 21-monooxygenase
Deficiency of steroid 21-monooxygenase 		54 0 5 2.5E-02 0 0
CUI: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency 		55 0 5 2.5E-02 0 0
CUI: C0008533
Disease: Hemophilia B
Hemophilia B 		59 0 5 2.5E-02 0 0
CUI: C3495436
Disease: American cutaneous leishmaniasis
American cutaneous leishmaniasis 		19 0 4 2.4E-02 0 0
CUI: C0009782
Disease: Connective Tissue Diseases
Connective Tissue Diseases 		188 0 8 2.4E-02 0 0