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: C1857632
Disease: Narrow palm
Narrow palm 		17 0 1 3.2E-04 0 0
CUI: C1883529
Disease: Ventricular Arrhythmia, CTCAE 3.0
Ventricular Arrhythmia, CTCAE 3.0 		17 0 1 3.2E-04 0 0
CUI: C3897558
Disease: Soluble Interleukin 6 Receptor Measurement
Soluble Interleukin 6 Receptor Measurement 		17 0 1 3.2E-04 0 0
CUI: C4553764
Disease: Ventricular Arrhythmia, CTCAE 5.0
Ventricular Arrhythmia, CTCAE 5.0 		17 0 1 3.2E-04 0 0
CUI: C0020599
Disease: Hypocalciuria
Hypocalciuria 		16 0 1 3.2E-04 0 0
CUI: C0036069
Disease: Saldino-Noonan Syndrome
Saldino-Noonan Syndrome 		16 0 1 3.2E-04 0 0
CUI: C0158551
Disease: Embryonal nuclear cataract (disorder)
Embryonal nuclear cataract (disorder) 		16 0 1 3.2E-04 0 0
CUI: C0201952
Disease: Chloride measurement
Chloride measurement 		16 0 1 3.2E-04 0 0
CUI: C0393556
Disease: Complicated hereditary spastic paraplegia
Complicated hereditary spastic paraplegia 		16 0 1 3.2E-04 0 0
CUI: C1837899
Disease: Type I transferrin isoform profile
Type I transferrin isoform profile 		16 0 1 3.2E-04 0 0
CUI: C1843865
Disease: Vestibular dysfunction
Vestibular dysfunction 		16 0 1 3.2E-04 0 0
CUI: C1859722
Disease: Arthrogryposis, renal dysfunction, and cholestasis 1
Arthrogryposis, renal dysfunction, and cholestasis 1 		16 0 1 3.2E-04 0 0
CUI: C1866021
Disease: Increased connective tissue
Increased connective tissue 		16 0 1 3.2E-04 0 0
CUI: C2931850
Disease: Aase Smith syndrome 2
Aase Smith syndrome 2 		16 0 1 3.2E-04 0 0
CUI: C3279547
Disease: Hypergranulosis
Hypergranulosis 		16 0 1 3.2E-04 0 0
CUI: C3279725
Disease: Hip flexor weakness
Hip flexor weakness 		16 0 1 3.2E-04 0 0
CUI: C3809827
Disease: Staring gaze
Staring gaze 		16 0 1 3.2E-04 0 0
CUI: C4025858
Disease: Abnormal cochlea morphology
Abnormal cochlea morphology 		16 0 1 3.2E-04 0 0
CUI: C0008711
Disease: Chronic rhinitis
Chronic rhinitis 		15 0 1 3.2E-04 0 0
CUI: C0221209
Disease: Pelvic kidney
Pelvic kidney 		15 0 1 3.2E-04 0 0
CUI: C0752207
Disease: Familial Dystonia
Familial Dystonia 		15 0 1 3.2E-04 0 0
CUI: C1142132
Disease: Carnitine deficiency
Carnitine deficiency 		15 0 1 3.2E-04 0 0
CUI: C2825857
Disease: Factor VIII measurement
Factor VIII measurement 		15 0 1 3.2E-04 0 0
CUI: C2936406
Disease: alpha-Dystroglycanopathies
alpha-Dystroglycanopathies 		15 0 1 3.2E-04 0 0
CUI: C3278322
Disease: Cerebellar dysplasia
Cerebellar dysplasia 		15 0 1 3.2E-04 0 0