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: C0010334
Disease: Crisscross Heart
Crisscross Heart 		1 0 1 0.20 0 0
CUI: C0232259
Disease: Mid-systolic murmur
Mid-systolic murmur 		1 0 1 0.20 0 0
CUI: C0267494
Disease: Chilaiditi Syndrome
Chilaiditi Syndrome 		1 0 1 0.20 0 0
CUI: C0349477
Disease: Transient neonatal hypothyroidism
Transient neonatal hypothyroidism 		1 0 1 0.20 0 0
CUI: C0409939
Disease: Osteoarthritis of glenohumeral joint
Osteoarthritis of glenohumeral joint 		1 0 1 0.20 0 0
CUI: C0410165
Disease: X-linked muscular dystrophy with abnormal dystrophin
X-linked muscular dystrophy with abnormal dystrophin 		1 0 1 0.20 0 0
CUI: C0553668
Disease: Labored breathing
Labored breathing 		1 0 1 0.20 0 0
CUI: C0699741
Disease: Benign congenital myopathy
Benign congenital myopathy 		1 0 1 0.20 0 0
CUI: C1834056
Disease: Thin anteverted nares
Thin anteverted nares 		1 0 1 0.20 0 0
CUI: C1834057
Disease: Vertebral hyperostosis
Vertebral hyperostosis 		1 0 1 0.20 0 0
CUI: C1843632
Disease: LEPROSY, SUSCEPTIBILITY TO, 2
LEPROSY, SUSCEPTIBILITY TO, 2 		1 0 1 0.20 0 0
CUI: C1857508
Disease: Patchy sclerosis of finger phalanx
Patchy sclerosis of finger phalanx 		1 0 1 0.20 0 0
CUI: C1861366
Disease: SYNDACTYLY, TYPE III
SYNDACTYLY, TYPE III 		1 0 1 0.20 0 0
CUI: C1863093
Disease: Alopecia congenita keratosis palmoplantaris
Alopecia congenita keratosis palmoplantaris 		1 0 1 0.20 0 0
CUI: C1970859
Disease: Atypical Mycobacteriosis, Familial, X-Linked 2
Atypical Mycobacteriosis, Familial, X-Linked 2 		1 0 1 0.20 0 0
CUI: C2749477
Disease: Oculodentodigital Dysplasia, Autosomal Recessive
Oculodentodigital Dysplasia, Autosomal Recessive 		1 0 1 0.20 0 0
CUI: C2875313
Disease: Severe [Duchenne] muscular dystrophy
Severe [Duchenne] muscular dystrophy 		1 0 1 0.20 0 0
CUI: C2931577
Disease: Basaran Yilmaz syndrome
Basaran Yilmaz syndrome 		1 0 1 0.20 0 0
CUI: C3151468
Disease: PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 1
PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 1 		1 0 1 0.20 0 0
CUI: C3275750
Disease: ATRIOVENTRICULAR SEPTAL DEFECT 3
ATRIOVENTRICULAR SEPTAL DEFECT 3 		1 0 1 0.20 0 0
CUI: C3277750
Disease: Absent middle phalanx of 5th finger
Absent middle phalanx of 5th finger 		1 0 1 0.20 0 0
CUI: C3844818
Disease: Attention Deficit Hyper Activity
Attention Deficit Hyper Activity 		1 0 1 0.20 0 0
CUI: C4016476
Disease: DUCHENNE MUSCULAR DYSTROPHY, MENTAL RETARDATION, AND ABSENCE OF ERG B-WAVE
DUCHENNE MUSCULAR DYSTROPHY, MENTAL RETARDATION, AND ABSENCE OF ERG B-WAVE 		1 0 1 0.20 0 0
CUI: C4016477
Disease: INTERMEDIATE MUSCULAR DYSTROPHY
INTERMEDIATE MUSCULAR DYSTROPHY 		1 0 1 0.20 0 0
CUI: C4021622
Disease: 2-4 toe cutaneous syndactyly
2-4 toe cutaneous syndactyly 		1 0 1 0.20 0 0