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: C0017412
Disease: Genital Diseases, Male
Genital Diseases, Male 		1 0 1 2.2E-02 0 0
CUI: C0037188
Disease: Sinoatrial Block
Sinoatrial Block 		1 0 1 2.2E-02 0 0
CUI: C0233480
Disease: Hyperirritability
Hyperirritability 		1 0 1 2.2E-02 0 0
CUI: C0235832
Disease: Congenital hernia
Congenital hernia 		1 0 1 2.2E-02 0 0
CUI: C0236099
Disease: Disorder of male reproductive system
Disorder of male reproductive system 		1 0 1 2.2E-02 0 0
CUI: C0266430
Disease: Polyorchism
Polyorchism 		1 0 1 2.2E-02 0 0
CUI: C0267494
Disease: Chilaiditi Syndrome
Chilaiditi Syndrome 		1 0 1 2.2E-02 0 0
CUI: C0267548
Disease: Ileocolic intussusception
Ileocolic intussusception 		1 0 1 2.2E-02 0 0
CUI: C0342530
Disease: Incomplete testicular feminization syndrome
Incomplete testicular feminization syndrome 		1 0 1 2.2E-02 0 0
CUI: C0406482
Disease: Nodulocystic acne
Nodulocystic acne 		1 0 1 2.2E-02 0 0
CUI: C0410165
Disease: X-linked muscular dystrophy with abnormal dystrophin
X-linked muscular dystrophy with abnormal dystrophin 		1 0 1 2.2E-02 0 0
CUI: C0454643
Disease: Word finding difficulty (disorder)
Word finding difficulty (disorder) 		1 0 1 2.2E-02 0 0
CUI: C0555197
Disease: Florid cemento-osseous dysplasia
Florid cemento-osseous dysplasia 		1 0 1 2.2E-02 0 0
CUI: C0558384
Disease: Arthritis/arthrosis
Arthritis/arthrosis 		1 0 1 2.2E-02 0 0
CUI: C0699741
Disease: Benign congenital myopathy
Benign congenital myopathy 		1 0 1 2.2E-02 0 0
CUI: C0751059
Disease: Cranial Neuropathies, Multiple
Cranial Neuropathies, Multiple 		1 0 1 2.2E-02 0 0
CUI: C0752353
Disease: Atrophy, Muscular, Spinobulbar
Atrophy, Muscular, Spinobulbar 		1 0 1 2.2E-02 0 0
CUI: C0795865
Disease: Chromosome 17, trisomy 17p
Chromosome 17, trisomy 17p 		1 0 1 2.2E-02 0 0
CUI: C0796031
Disease: Malouf syndrome
Malouf syndrome 		1 0 1 2.2E-02 0 0
CUI: C0796083
Disease: Najjar syndrome
Najjar syndrome 		1 0 1 2.2E-02 0 0
CUI: C0860159
Disease: Partial androgen resistance
Partial androgen resistance 		1 0 1 2.2E-02 0 0
CUI: C0865181
Disease: Female Virilization
Female Virilization 		1 0 1 2.2E-02 0 0
CUI: C1695985
Disease: Lewis-Sumner syndrome
Lewis-Sumner syndrome 		1 0 1 2.2E-02 0 0
CUI: C1834460
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10 		1 0 1 2.2E-02 0 0
CUI: C1834559
Disease: Continuous Muscle Fiber Activity, Hereditary
Continuous Muscle Fiber Activity, Hereditary 		1 0 1 2.2E-02 0 0