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: C0234860
Disease: Weak cry
Weak cry 		42 0 10 0.11 0 0
CUI: C1527344
Disease: Dysphonia
Dysphonia 		77 0 13 0.11 0 0
CUI: C0345392
Disease: Congenital kyphoscoliosis
Congenital kyphoscoliosis 		151 0 20 0.11 0 0
CUI: C0751882
Disease: Myasthenic Syndromes, Congenital
Myasthenic Syndromes, Congenital 		57 0 11 0.11 0 0
CUI: C0221629
Disease: Proximal muscle weakness
Proximal muscle weakness 		112 0 16 0.10 0 0
CUI: C0600033
Disease: Acquired Kyphoscoliosis
Acquired Kyphoscoliosis 		149 0 19 0.10 0 0
CUI: C1848736
Disease: Distal amyotrophy
Distal amyotrophy 		106 0 15 0.10 0 0
CUI: C1839546
Disease: Microretrognathia
Microretrognathia 		53 0 10 9.9E-02 0 0
CUI: C0010520
Disease: Cyanosis
Cyanosis 		54 0 10 9.8E-02 0 0
CUI: C0575158
Disease: Kyphoscoliosis deformity of spine
Kyphoscoliosis deformity of spine 		155 0 19 9.8E-02 0 0
CUI: C0740418
Disease: Chronic back pain
Chronic back pain 		10 0 6 9.7E-02 0 0
CUI: C3278509
Disease: Spinal fusion
Spinal fusion 		67 0 11 9.6E-02 0 0
CUI: C1184923
Disease: Lumbar hyperlordosis
Lumbar hyperlordosis 		92 0 13 9.5E-02 0 0
CUI: C0566620
Disease: Nasal voice
Nasal voice 		93 0 13 9.4E-02 0 0
CUI: C0012569
Disease: Diplopia
Diplopia 		75 0 11 9.0E-02 0 0
CUI: C0231712
Disease: Waddling gait
Waddling gait 		113 0 14 8.9E-02 0 0
CUI: C0158731
Disease: Congenital pectus carinatum
Congenital pectus carinatum 		138 0 16 8.9E-02 0 0
CUI: C4021726
Disease: EMG: myopathic abnormalities
EMG: myopathic abnormalities 		115 0 14 8.8E-02 0 0
CUI: C0038017
Disease: Congenital spondylolisthesis
Congenital spondylolisthesis 		17 0 6 8.7E-02 0 0
CUI: C4073139
Disease: Abnormality of the tongue muscle
Abnormality of the tongue muscle 		5 0 5 8.6E-02 0 0
CUI: C0751883
Disease: Congenital Myasthenic Syndromes, Postsynaptic
Congenital Myasthenic Syndromes, Postsynaptic 		18 0 6 8.6E-02 0 0
CUI: C0751885
Disease: Myasthenic Syndromes, Congenital, Slow Channel
Myasthenic Syndromes, Congenital, Slow Channel 		18 0 6 8.6E-02 0 0
CUI: C0234146
Disease: Absent reflex
Absent reflex 		201 0 20 8.4E-02 0 0
CUI: C1843057
Disease: Calf muscle hypertrophy
Calf muscle hypertrophy 		46 0 8 8.3E-02 0 0
CUI: C4024905
Disease: Abnormality of the pons
Abnormality of the pons 		7 0 5 8.3E-02 0 0