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: C0234244
Disease: Tissue Pain
Tissue Pain 		1 0 1 0.20 0 0
CUI: C0264081
Disease: Osteoarthropathy of fingers familial
Osteoarthropathy of fingers familial 		1 0 1 0.20 0 0
CUI: C0265280
Disease: Spondylometaphyseal dysplasia, Kozlowski type
Spondylometaphyseal dysplasia, Kozlowski type 		1 11 1 0.20 3 0.14
CUI: C0265281
Disease: Metatropic dwarfism
Metatropic dwarfism 		1 19 1 0.20 2 6.7E-02
CUI: C0432227
Disease: Brachyolmia Type 3
Brachyolmia Type 3 		1 3 1 0.20 2 0.14
CUI: C0562557
Disease: Sexually disinhibited behavior
Sexually disinhibited behavior 		1 0 1 0.20 0 0
CUI: C1838492
Disease: SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE (disorder)
SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE (disorder) 		1 6 1 0.20 5 0.36
CUI: C1842197
Disease: Charcot-Marie-Tooth Disease, Recessive Intermediate A
Charcot-Marie-Tooth Disease, Recessive Intermediate A 		1 0 1 0.20 0 0
CUI: C1842984
Disease: Charcot-Marie-Tooth Disease, Autosomal Dominant, Type 2k
Charcot-Marie-Tooth Disease, Autosomal Dominant, Type 2k 		1 0 1 0.20 0 0
CUI: C1847406
Disease: Digital Arthropathy-Brachydactyly, Familial
Digital Arthropathy-Brachydactyly, Familial 		1 4 1 0.20 1 6.2E-02
CUI: C1847408
Disease: Brachytelomesophalangy
Brachytelomesophalangy 		1 0 1 0.20 0 0
CUI: C1861678
Disease: Charcot-Marie-Tooth Disease, Axonal, Type 2a1
Charcot-Marie-Tooth Disease, Axonal, Type 2a1 		1 0 1 0.20 0 0
CUI: C1866703
Disease: Severe carpal ossification delay
Severe carpal ossification delay 		1 0 1 0.20 0 0
CUI: C1868616
Disease: Parastremmatic dwarfism
Parastremmatic dwarfism 		1 2 1 0.20 2 0.15
CUI: C2079540
Disease: Charcot-Marie-Tooth disease, Type 2C
Charcot-Marie-Tooth disease, Type 2C 		1 0 1 0.20 0 0
CUI: C3148833
Disease: Childhood-onset short-trunk short stature
Childhood-onset short-trunk short stature 		1 0 1 0.20 0 0
CUI: C3150755
Disease: SODIUM SERUM LEVEL QUANTITATIVE TRAIT LOCUS 1
SODIUM SERUM LEVEL QUANTITATIVE TRAIT LOCUS 1 		1 1 1 0.20 1 7.7E-02
CUI: C3159322
Disease: SPONDYLOEPIPHYSEAL DYSPLASIA, MAROTEAUX TYPE
SPONDYLOEPIPHYSEAL DYSPLASIA, MAROTEAUX TYPE 		1 5 1 0.20 2 0.12
CUI: C3277114
Disease: Relatively short spine
Relatively short spine 		1 0 1 0.20 0 0
CUI: C3277116
Disease: Long coccyx
Long coccyx 		1 0 1 0.20 0 0
CUI: C3277119
Disease: Halberd-shaped pelvis
Halberd-shaped pelvis 		1 0 1 0.20 0 0
CUI: C3277120
Disease: Hyperplasia of the femoral trochanters
Hyperplasia of the femoral trochanters 		1 0 1 0.20 0 0
CUI: C3277123
Disease: Dumbbell-shaped metaphyses
Dumbbell-shaped metaphyses 		1 0 1 0.20 0 0
CUI: C3277126
Disease: Absent primary metaphyseal spongiosa
Absent primary metaphyseal spongiosa 		1 0 1 0.20 0 0
CUI: C3277127
Disease: Abnormal metaphyseal vascular invasion
Abnormal metaphyseal vascular invasion 		1 0 1 0.20 0 0