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: C1456418
Disease: Absence of muscle
Absence of muscle 		0 2 0 0 1 6.2E-02
CUI: C0264963
Disease: Aneurysm of femoral artery
Aneurysm of femoral artery 		1 0 1 4.5E-02 0 0
CUI: C0265878
Disease: Preductal coarctation of aorta
Preductal coarctation of aorta 		1 0 1 4.5E-02 0 0
CUI: C0268875
Disease: Urethrorectal fistula
Urethrorectal fistula 		1 0 1 4.5E-02 0 0
CUI: C0270149
Disease: Perinatal respiratory distress
Perinatal respiratory distress 		1 0 1 4.5E-02 0 0
CUI: C0423729
Disease: Chest pain on breathing
Chest pain on breathing 		1 0 1 4.5E-02 0 0
CUI: C0742794
Disease: Multiple contractures
Multiple contractures 		1 0 1 4.5E-02 0 0
CUI: C1112616
Disease: Loss of proprioception
Loss of proprioception 		1 0 1 4.5E-02 0 0
CUI: C1411006
Disease: Finger contracture
Finger contracture 		1 0 1 4.5E-02 0 0
CUI: C1456270
Disease: Fatty acid oxidation disorder
Fatty acid oxidation disorder 		1 0 1 4.5E-02 0 0
CUI: C1836447
Disease: Nemaline myopathy 4
Nemaline myopathy 4 		1 9 1 4.5E-02 1 4.3E-02
CUI: C1840365
Disease: King Denborough syndrome
King Denborough syndrome 		1 0 1 4.5E-02 0 0
CUI: C1841686
Disease: Absent hallux
Absent hallux 		1 0 1 4.5E-02 0 0
CUI: C1848473
Disease: Whistling appearance
Whistling appearance 		1 0 1 4.5E-02 0 0
CUI: C1855003
Disease: Bilateral postaxial polydactyly
Bilateral postaxial polydactyly 		1 0 1 4.5E-02 0 0
CUI: C1860081
Disease: Medium chain dicarboxylic aciduria
Medium chain dicarboxylic aciduria 		1 0 1 4.5E-02 0 0
CUI: C1860309
Disease: Chin with H-shaped crease
Chin with H-shaped crease 		1 0 1 4.5E-02 0 0
CUI: C1861753
Disease: Multiminicore Disease, Moderate, with Hand Involvement
Multiminicore Disease, Moderate, with Hand Involvement 		1 0 1 4.5E-02 0 0
CUI: C1862491
Disease: Internally rotated shoulders
Internally rotated shoulders 		1 0 1 4.5E-02 0 0
CUI: C1867440
Disease: Multiple Pterygium Syndrome, Autosomal Dominant
Multiple Pterygium Syndrome, Autosomal Dominant 		1 0 1 4.5E-02 0 0
CUI: C1868111
Disease: Polydactyly, preaxial 4
Polydactyly, preaxial 4 		1 0 1 4.5E-02 0 0
CUI: C1968943
Disease: Rudimentary to absent tibiae
Rudimentary to absent tibiae 		1 0 1 4.5E-02 0 0
CUI: C2083352
Disease: Rectus femoris muscle atrophy
Rectus femoris muscle atrophy 		1 0 1 4.5E-02 0 0
CUI: C2674259
Disease: NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER (disorder)
NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER (disorder) 		1 0 1 4.5E-02 0 0
CUI: C2675191
Disease: Polymicrogyria, Bilateral Occipital
Polymicrogyria, Bilateral Occipital 		1 0 1 4.5E-02 0 0