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: C0043352
Disease: Xerostomia
Xerostomia 		56 0 1 1.8E-02 0 0
CUI: C4552072
Disease: X-linked infantile spasms
X-linked infantile spasms 		53 0 1 1.9E-02 0 0
CUI: C3178789
Disease: Widespread Chronic Pain
Widespread Chronic Pain 		19 0 1 5.0E-02 0 0
CUI: C0042384
Disease: Vasculitis
Vasculitis 		294 0 1 3.4E-03 0 0
CUI: C1861403
Disease: Variable expressivity
Variable expressivity 		319 0 1 3.1E-03 0 0
CUI: C0042024
Disease: Urinary Incontinence
Urinary Incontinence 		151 0 1 6.6E-03 0 0
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion 		6626 0 1 1.5E-04 0 0
CUI: C0040822
Disease: Tremor
Tremor 		528 0 1 1.9E-03 0 0
CUI: C0270844
Disease: Tonic Seizures
Tonic Seizures 		108 0 1 9.2E-03 0 0
CUI: C0494475
Disease: Tonic - clonic seizures
Tonic - clonic seizures 		300 0 1 3.3E-03 0 0
CUI: C0426900
Disease: Tibial torsion
Tibial torsion 		12 0 1 7.7E-02 0 0
CUI: C0426886
Disease: Tapering fingers (finding)
Tapering fingers (finding) 		91 0 1 1.1E-02 0 0
CUI: C1301937
Disease: Talipes
Talipes 		74 0 1 1.3E-02 0 0
CUI: C0039231
Disease: Tachycardia
Tachycardia 		73 0 1 1.4E-02 0 0
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		979 0 1 1.0E-03 0 0
CUI: C0338479
Disease: Symptomatic Myoclonic Epilepsy
Symptomatic Myoclonic Epilepsy 		8 0 1 0.11 0 0
CUI: C0011071
Disease: Sudden death
Sudden death 		30 0 1 3.2E-02 0 0
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		3720 0 1 2.7E-04 0 0
CUI: C0038220
Disease: Status Epilepticus
Status Epilepticus 		533 0 1 1.9E-03 0 0
CUI: C0241210
Disease: Speech Delay
Speech Delay 		58 0 1 1.7E-02 0 0
CUI: C0037650
Disease: Somatoform Disorder
Somatoform Disorder 		2 0 1 0.33 0 0
CUI: C3276706
Disease: Small Fiber Neuropathy
Small Fiber Neuropathy 		35 0 2 5.7E-02 0 0
CUI: C1854494
Disease: Slow progression
Slow progression 		165 0 1 6.0E-03 0 0
CUI: C0541794
Disease: Skeletal muscle atrophy
Skeletal muscle atrophy 		306 0 1 3.3E-03 0 0
CUI: C0699739
Disease: Sensory Neuropathy, Hereditary
Sensory Neuropathy, Hereditary 		19 0 1 5.0E-02 0 0