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: C0155761
Disease: Hyperplasia of renal artery
Hyperplasia of renal artery 		1 0 1 0.50 0 0
CUI: C0156245
Disease: Unilateral small kidney
Unilateral small kidney 		1 0 1 0.50 0 0
CUI: C0234244
Disease: Tissue Pain
Tissue Pain 		1 0 1 0.50 0 0
CUI: C0264081
Disease: Osteoarthropathy of fingers familial
Osteoarthropathy of fingers familial 		1 0 1 0.50 0 0
CUI: C0264639
Disease: High-renin essential hypertension
High-renin essential hypertension 		1 0 1 0.50 0 0
CUI: C0264693
Disease: Acute coronary insufficiency
Acute coronary insufficiency 		1 0 1 0.50 0 0
CUI: C0265280
Disease: Spondylometaphyseal dysplasia, Kozlowski type
Spondylometaphyseal dysplasia, Kozlowski type 		1 0 1 0.50 0 0
CUI: C0265281
Disease: Metatropic dwarfism
Metatropic dwarfism 		1 0 1 0.50 0 0
CUI: C0432227
Disease: Brachyolmia Type 3
Brachyolmia Type 3 		1 0 1 0.50 0 0
CUI: C0521623
Disease: Kidney crystallization
Kidney crystallization 		1 0 1 0.50 0 0
CUI: C0562557
Disease: Sexually disinhibited behavior
Sexually disinhibited behavior 		1 0 1 0.50 0 0
CUI: C0877138
Disease: Osteopenia periarticular
Osteopenia periarticular 		1 0 1 0.50 0 0
CUI: C1301626
Disease: Hypertension with albuminuria
Hypertension with albuminuria 		1 0 1 0.50 0 0
CUI: C1838492
Disease: SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE (disorder)
SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE (disorder) 		1 0 1 0.50 0 0
CUI: C1847406
Disease: Digital Arthropathy-Brachydactyly, Familial
Digital Arthropathy-Brachydactyly, Familial 		1 0 1 0.50 0 0
CUI: C1847408
Disease: Brachytelomesophalangy
Brachytelomesophalangy 		1 0 1 0.50 0 0
CUI: C1866703
Disease: Severe carpal ossification delay
Severe carpal ossification delay 		1 0 1 0.50 0 0
CUI: C1868616
Disease: Parastremmatic dwarfism
Parastremmatic dwarfism 		1 0 1 0.50 0 0
CUI: C2063386
Disease: Left atrial appendage thrombosis
Left atrial appendage thrombosis 		1 0 1 0.50 0 0
CUI: C2079540
Disease: Charcot-Marie-Tooth disease, Type 2C
Charcot-Marie-Tooth disease, Type 2C 		1 0 1 0.50 0 0
CUI: C2902961
Disease: Page kidney
Page kidney 		1 0 1 0.50 0 0
CUI: C3148833
Disease: Childhood-onset short-trunk short stature
Childhood-onset short-trunk short stature 		1 0 1 0.50 0 0
CUI: C3150755
Disease: SODIUM SERUM LEVEL QUANTITATIVE TRAIT LOCUS 1
SODIUM SERUM LEVEL QUANTITATIVE TRAIT LOCUS 1 		1 0 1 0.50 0 0
CUI: C3159322
Disease: SPONDYLOEPIPHYSEAL DYSPLASIA, MAROTEAUX TYPE
SPONDYLOEPIPHYSEAL DYSPLASIA, MAROTEAUX TYPE 		1 0 1 0.50 0 0
CUI: C3277114
Disease: Relatively short spine
Relatively short spine 		1 0 1 0.50 0 0