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: C0016512
Disease: Foot pain
Foot pain 		1 0 1 2.6E-02 0 0
CUI: C0037188
Disease: Sinoatrial Block
Sinoatrial Block 		1 0 1 2.6E-02 0 0
CUI: C0267548
Disease: Ileocolic intussusception
Ileocolic intussusception 		1 0 1 2.6E-02 0 0
CUI: C0555197
Disease: Florid cemento-osseous dysplasia
Florid cemento-osseous dysplasia 		1 0 1 2.6E-02 0 0
CUI: C0558384
Disease: Arthritis/arthrosis
Arthritis/arthrosis 		1 0 1 2.6E-02 0 0
CUI: C0796031
Disease: Malouf syndrome
Malouf syndrome 		1 0 1 2.6E-02 0 0
CUI: C0796083
Disease: Najjar syndrome
Najjar syndrome 		1 0 1 2.6E-02 0 0
CUI: C1835093
Disease: Masticatory Muscles, Hypertrophy of
Masticatory Muscles, Hypertrophy of 		1 0 1 2.6E-02 0 0
CUI: C1835380
Disease: Labial pseudohypertrophy
Labial pseudohypertrophy 		1 0 1 2.6E-02 0 0
CUI: C1835389
Disease: Increased intramuscular fat
Increased intramuscular fat 		1 0 1 2.6E-02 0 0
CUI: C1836050
Disease: Filaminopathy, autosomal dominant
Filaminopathy, autosomal dominant 		1 0 1 2.6E-02 0 0
CUI: C1836447
Disease: Nemaline myopathy 4
Nemaline myopathy 4 		1 0 1 2.6E-02 0 0
CUI: C1836448
Disease: Nemaline myopathy 1
Nemaline myopathy 1 		1 0 1 2.6E-02 0 0
CUI: C1836472
Disease: Nemaline myopathy 6
Nemaline myopathy 6 		1 0 1 2.6E-02 0 0
CUI: C1836485
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2 (disorder)
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2 (disorder) 		1 0 1 2.6E-02 0 0
CUI: C1839028
Disease: Mitochondrial Myopathy with Diabetes
Mitochondrial Myopathy with Diabetes 		1 0 1 2.6E-02 0 0
CUI: C1840365
Disease: King Denborough syndrome
King Denborough syndrome 		1 0 1 2.6E-02 0 0
CUI: C1842062
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1F
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1F 		1 3 1 2.6E-02 1 0.20
CUI: C1843791
Disease: CARDIOMYOPATHY, DILATED, 1N
CARDIOMYOPATHY, DILATED, 1N 		1 0 1 2.6E-02 0 0
CUI: C1847532
Disease: MYOPATHY, DISTAL, WITH ANTERIOR TIBIAL ONSET
MYOPATHY, DISTAL, WITH ANTERIOR TIBIAL ONSET 		1 0 1 2.6E-02 0 0
CUI: C1854488
Disease: Spinocerebellar ataxia 13
Spinocerebellar ataxia 13 		1 0 1 2.6E-02 0 0
CUI: C1857829
Disease: Heart-hand syndrome, Slovenian type
Heart-hand syndrome, Slovenian type 		1 0 1 2.6E-02 0 0
CUI: C1861753
Disease: Multiminicore Disease, Moderate, with Hand Involvement
Multiminicore Disease, Moderate, with Hand Involvement 		1 0 1 2.6E-02 0 0
CUI: C1862133
Disease: Decreased finger mobility
Decreased finger mobility 		1 0 1 2.6E-02 0 0
CUI: C1866008
Disease: Muscular Dystrophy, Limb-Girdle, Type 2G
Muscular Dystrophy, Limb-Girdle, Type 2G 		1 0 1 2.6E-02 0 0