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: C0038940
Disease: Surgical Wound Dehiscence
Surgical Wound Dehiscence 		1 0 1 0.20 0 0
CUI: C1846010
Disease: URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME
URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME 		1 0 1 0.20 0 0
CUI: C2678015
Disease: Myopathy, Reducing Body, X-Linked, Childhood-Onset
Myopathy, Reducing Body, X-Linked, Childhood-Onset 		1 0 1 0.20 0 0
CUI: C2678027
Disease: Myopathy, Reducing Body, X-Linked, Early-Onset, Severe
Myopathy, Reducing Body, X-Linked, Early-Onset, Severe 		1 0 1 0.20 0 0
CUI: C2678055
Disease: MYOPATHY, X-LINKED, WITH POSTURAL MUSCLE ATROPHY (disorder)
MYOPATHY, X-LINKED, WITH POSTURAL MUSCLE ATROPHY (disorder) 		1 0 1 0.20 0 0
CUI: C2749106
Disease: Emery-Dreifuss Muscular Dystrophy 6, X-Linked
Emery-Dreifuss Muscular Dystrophy 6, X-Linked 		1 0 1 0.20 0 0
CUI: C3809004
Disease: CATARACT 19, MULTIPLE TYPES
CATARACT 19, MULTIPLE TYPES 		1 0 1 0.20 0 0
CUI: C3888197
Disease: LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 3
LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 3 		1 0 1 0.20 0 0
CUI: C4225159
Disease: REDUCING BODY MYOPATHY, X-LINKED 1B, WITH LATE CHILDHOOD OR ADULT ONSET
REDUCING BODY MYOPATHY, X-LINKED 1B, WITH LATE CHILDHOOD OR ADULT ONSET 		1 0 1 0.20 0 0
CUI: C4225423
Disease: REDUCING BODY MYOPATHY, X-LINKED 1A, SEVERE, WITH INFANTILE OR EARLY CHILDHOOD ONSET
REDUCING BODY MYOPATHY, X-LINKED 1A, SEVERE, WITH INFANTILE OR EARLY CHILDHOOD ONSET 		1 0 1 0.20 0 0
CUI: C0524912
Disease: Hepatitis, Chronic, Drug-Induced
Hepatitis, Chronic, Drug-Induced 		2 0 1 0.17 0 0
CUI: C1846011
Disease: Pugilistic facies
Pugilistic facies 		2 0 1 0.17 0 0
CUI: C4021568
Disease: Cortical pulverulent cataract
Cortical pulverulent cataract 		2 0 1 0.17 0 0
CUI: C1332578
Disease: Haemangioma of bone
Haemangioma of bone 		3 0 1 0.14 0 0
CUI: C1842161
Disease: Scapuloperoneal weakness
Scapuloperoneal weakness 		3 0 1 0.14 0 0
CUI: C1959626
Disease: Mevalonic Aciduria
Mevalonic Aciduria 		3 0 1 0.14 0 0
CUI: C2931268
Disease: Scapuloperoneal myopathy
Scapuloperoneal myopathy 		3 0 1 0.14 0 0
CUI: C3825297
Disease: Congenital heart disease in children
Congenital heart disease in children 		3 0 1 0.14 0 0
CUI: C0009438
Disease: Common Bile Duct Calculi
Common Bile Duct Calculi 		4 0 1 0.12 0 0
CUI: C0265910
Disease: Congenital hypoplasia of pulmonary artery
Congenital hypoplasia of pulmonary artery 		4 0 1 0.12 0 0
CUI: C0342467
Disease: Late onset congenital adrenal hyperplasia
Late onset congenital adrenal hyperplasia 		4 0 1 0.12 0 0
CUI: C1846013
Disease: Marked muscular hypertrophy
Marked muscular hypertrophy 		4 0 1 0.12 0 0
CUI: C3715147
Disease: Necrotising myositis
Necrotising myositis 		4 0 1 0.12 0 0
CUI: C4302167
Disease: Autoimmune myopathy
Autoimmune myopathy 		4 0 1 0.12 0 0
CUI: C0398777
Disease: Complement Factor H Deficiency
Complement Factor H Deficiency 		5 0 1 0.11 0 0