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: C0575158
Disease: Kyphoscoliosis deformity of spine
Kyphoscoliosis deformity of spine 		155 17 41 0.13 3 6.5E-02
CUI: C0600033
Disease: Acquired Kyphoscoliosis
Acquired Kyphoscoliosis 		149 0 40 0.13 0 0
CUI: C0345392
Disease: Congenital kyphoscoliosis
Congenital kyphoscoliosis 		151 0 40 0.12 0 0
CUI: C0240635
Disease: Byzanthine arch palate
Byzanthine arch palate 		497 70 73 0.12 5 5.2E-02
CUI: C0221629
Disease: Proximal muscle weakness
Proximal muscle weakness 		112 0 33 0.11 0 0
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified 		850 135 107 0.11 11 7.1E-02
CUI: C0024003
Disease: Lordosis
Lordosis 		160 0 37 0.11 0 0
CUI: C1854301
Disease: Motor delay
Motor delay 		384 34 57 0.11 1 1.5E-02
CUI: C4021726
Disease: EMG: myopathic abnormalities
EMG: myopathic abnormalities 		115 0 31 0.11 0 0
CUI: C0520947
Disease: Clumsiness - motor delay
Clumsiness - motor delay 		393 0 57 0.10 0 0
CUI: C1858025
Disease: Spinal rigidity
Spinal rigidity 		55 0 25 0.10 0 0
CUI: C0016202
Disease: Flatfoot
Flatfoot 		285 38 45 1.0E-01 6 9.4E-02
CUI: C2267233
Disease: Neonatal Hypotonia
Neonatal Hypotonia 		169 0 34 9.9E-02 0 0
CUI: C0541794
Disease: Skeletal muscle atrophy
Skeletal muscle atrophy 		306 0 46 9.8E-02 0 0
CUI: C0026826
Disease: Muscle Hypertonia
Muscle Hypertonia 		197 21 36 9.7E-02 3 6.0E-02
CUI: C0235659
Disease: Reduced fetal movement
Reduced fetal movement 		169 17 33 9.5E-02 1 2.1E-02
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties 		473 62 59 9.5E-02 2 2.2E-02
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios 		208 28 36 9.4E-02 2 3.4E-02
CUI: C0022821
Disease: Kyphosis deformity of spine
Kyphosis deformity of spine 		305 10 44 9.3E-02 1 2.4E-02
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		967 579 100 9.3E-02 3 4.9E-03
CUI: C0241005
Disease: Creatine phosphokinase serum increased
Creatine phosphokinase serum increased 		228 43 37 9.2E-02 1 1.4E-02
CUI: C0270960
Disease: Congenital myopathy (disorder)
Congenital myopathy (disorder) 		63 0 23 9.2E-02 0 0
CUI: C0025990
Disease: Micrognathism
Micrognathism 		586 53 67 9.2E-02 3 3.7E-02
CUI: C0026034
Disease: Microstomia
Microstomia 		172 9 32 9.1E-02 1 2.5E-02
CUI: C0162298
Disease: Joint stiffness
Joint stiffness 		163 0 31 9.1E-02 0 0