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: C0685787
Disease: Cleft face
Cleft face 		23 0 1 4.7E-04 0 0
CUI: C1568247
Disease: Usher Syndrome, Type I
Usher Syndrome, Type I 		23 0 1 4.7E-04 0 0
CUI: C4023683
Disease: EEG with spike-wave complexes
EEG with spike-wave complexes 		23 0 1 4.7E-04 0 0
CUI: C0000921
Disease: Accidental Falls
Accidental Falls 		22 0 1 4.8E-04 0 0
CUI: C3278811
Disease: Thumb aplasia
Thumb aplasia 		22 0 1 4.8E-04 0 0
CUI: C0036454
Disease: Scotoma
Scotoma 		21 0 1 4.8E-04 0 0
CUI: C0241391
Disease: Thumb absent
Thumb absent 		21 0 1 4.8E-04 0 0
CUI: C0272002
Disease: alpha^0^ Thalassemia
alpha^0^ Thalassemia 		21 0 1 4.8E-04 0 0
CUI: C0311277
Disease: Obesity, Abdominal
Obesity, Abdominal 		21 0 1 4.8E-04 0 0
CUI: C0743332
Disease: Focal Dystonia
Focal Dystonia 		21 0 1 4.8E-04 0 0
CUI: C1843920
Disease: COENZYME Q10 DEFICIENCY
COENZYME Q10 DEFICIENCY 		21 0 1 4.8E-04 0 0
CUI: C1844945
Disease: Episodic respiratory distress
Episodic respiratory distress 		21 0 1 4.8E-04 0 0
CUI: C3658299
Disease: Zellweger Spectrum
Zellweger Spectrum 		21 0 1 4.8E-04 0 0
CUI: C3894553
Disease: response to simvastatin
response to simvastatin 		21 0 1 4.8E-04 0 0
CUI: C4024809
Disease: Chorioretinal dysplasia
Chorioretinal dysplasia 		21 0 1 4.8E-04 0 0
CUI: C0002514
Disease: Amino Acid Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors 		20 0 1 4.8E-04 0 0
CUI: C0024507
Disease: Majewski Syndrome
Majewski Syndrome 		20 0 1 4.8E-04 0 0
CUI: C0403553
Disease: Renal dysplasia and retinal aplasia (disorder)
Renal dysplasia and retinal aplasia (disorder) 		20 0 1 4.8E-04 0 0
CUI: C1845123
Disease: Generalized neonatal hypotonia
Generalized neonatal hypotonia 		20 0 1 4.8E-04 0 0
CUI: C1860475
Disease: Retinal vascular tortuosity
Retinal vascular tortuosity 		20 0 1 4.8E-04 0 0
CUI: C2936862
Disease: Bardet-Biedl syndrome 1 (disorder)
Bardet-Biedl syndrome 1 (disorder) 		20 0 1 4.8E-04 0 0
CUI: C4021254
Disease: Cutaneous finger syndactyly
Cutaneous finger syndactyly 		20 0 1 4.8E-04 0 0
CUI: C4022735
Disease: Cerebral white matter atrophy
Cerebral white matter atrophy 		20 0 1 4.8E-04 0 0
CUI: C4551520
Disease: Intention tremor
Intention tremor 		20 0 1 4.8E-04 0 0
CUI: C0011432
Disease: Dentin Sensitivity
Dentin Sensitivity 		19 0 1 4.8E-04 0 0