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: C0033893
Disease: Tension Headache
Tension Headache 		12 6 3 0.10 1 4.2E-02
CUI: C0024528
Disease: Malaise and fatigue
Malaise and fatigue 		2 1 2 1.0E-01 1 5.3E-02
CUI: C0494479
Disease: Other headache syndrome
Other headache syndrome 		2 1 2 1.0E-01 1 5.3E-02
CUI: C1367972
Disease: Phlebitis and thrombophlebitis
Phlebitis and thrombophlebitis 		2 1 2 1.0E-01 1 5.3E-02
CUI: C0449439
Disease: Carrier status
Carrier status 		3 0 2 9.5E-02 0 0
CUI: C3804968
Disease: Pathergy reaction
Pathergy reaction 		3 0 2 9.5E-02 0 0
CUI: C0030196
Disease: Pain in limb
Pain in limb 		16 5 3 9.1E-02 3 0.14
CUI: C0155943
Disease: Arthralgia of temporomandibular joint
Arthralgia of temporomandibular joint 		4 0 2 9.1E-02 0 0
CUI: C0546817
Disease: Fluid overload
Fluid overload 		4 1 2 9.1E-02 1 5.3E-02
CUI: C2986662
Disease: Multifocal breast carcinoma
Multifocal breast carcinoma 		5 0 2 8.7E-02 0 0
CUI: C3277671
Disease: THROMBOCYTHEMIA 1
THROMBOCYTHEMIA 1 		5 4 2 8.7E-02 1 4.5E-02
CUI: C0751466
Disease: Phonophobia
Phonophobia 		18 0 3 8.6E-02 0 0
CUI: C0009197
Disease: Cochlear Diseases
Cochlear Diseases 		6 0 2 8.3E-02 0 0
CUI: C0201910
Disease: Beta-2-microglobulin measurement
Beta-2-microglobulin measurement 		6 0 2 8.3E-02 0 0
CUI: C0392998
Disease: Carcinosarcoma of ovary
Carcinosarcoma of ovary 		6 0 2 8.3E-02 0 0
CUI: C0740421
Disease: Postsurgical menopause
Postsurgical menopause 		6 0 2 8.3E-02 0 0
CUI: C1332355
Disease: Autoimmune Hepatitis with Centrilobular Necrosis
Autoimmune Hepatitis with Centrilobular Necrosis 		6 0 2 8.3E-02 0 0
CUI: C0001422
Disease: Adenofibroma
Adenofibroma 		8 0 2 7.7E-02 0 0
CUI: C0029823
Disease: Other specified peritonitis
Other specified peritonitis 		8 0 2 7.7E-02 0 0
CUI: C0917715
Disease: Hajdu-Cheney Syndrome
Hajdu-Cheney Syndrome 		8 0 2 7.7E-02 0 0
CUI: C0338484
Disease: Familial Hemiplegic Migraine
Familial Hemiplegic Migraine 		24 0 3 7.3E-02 0 0
CUI: C1836843
Disease: Progressive inability to walk
Progressive inability to walk 		10 3 2 7.1E-02 1 4.8E-02
CUI: C2364016
Disease: Systemic sclerosis [scleroderma]
Systemic sclerosis [scleroderma] 		11 0 2 6.9E-02 0 0
CUI: C0012754
Disease: Distemper
Distemper 		12 0 2 6.7E-02 0 0
CUI: C0342345
Disease: Hypoparathyroidism - autosomal dominant
Hypoparathyroidism - autosomal dominant 		12 0 2 6.7E-02 0 0