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: C0520886
Disease: ST segment elevation (finding)
ST segment elevation (finding) 		23 0 1 3.7E-04 0 0
CUI: C1568247
Disease: Usher Syndrome, Type I
Usher Syndrome, Type I 		23 0 1 3.7E-04 0 0
CUI: C0000921
Disease: Accidental Falls
Accidental Falls 		22 0 1 3.7E-04 0 0
CUI: C0036454
Disease: Scotoma
Scotoma 		21 0 1 3.7E-04 0 0
CUI: C0237849
Disease: Peeling of skin
Peeling of skin 		21 0 1 3.7E-04 0 0
CUI: C0272002
Disease: alpha^0^ Thalassemia
alpha^0^ Thalassemia 		21 0 1 3.7E-04 0 0
CUI: C1834536
Disease: Weakness of the intrinsic hand muscles
Weakness of the intrinsic hand muscles 		21 0 1 3.7E-04 0 0
CUI: C1844945
Disease: Episodic respiratory distress
Episodic respiratory distress 		21 0 1 3.7E-04 0 0
CUI: C3894553
Disease: response to simvastatin
response to simvastatin 		21 0 1 3.7E-04 0 0
CUI: C4024809
Disease: Chorioretinal dysplasia
Chorioretinal dysplasia 		21 0 1 3.7E-04 0 0
CUI: C0034880
Disease: Hyperacusis
Hyperacusis 		20 0 1 3.7E-04 0 0
CUI: C0403553
Disease: Renal dysplasia and retinal aplasia (disorder)
Renal dysplasia and retinal aplasia (disorder) 		20 0 1 3.7E-04 0 0
CUI: C3468114
Disease: Juvenile amyotrophic lateral sclerosis
Juvenile amyotrophic lateral sclerosis 		20 0 1 3.7E-04 0 0
CUI: C0343073
Disease: Wooly hair
Wooly hair 		19 0 1 3.7E-04 0 0
CUI: C0457133
Disease: Muscle eye brain disease
Muscle eye brain disease 		19 0 1 3.7E-04 0 0
CUI: C0751884
Disease: Congenital Myasthenic Syndromes, Presynaptic
Congenital Myasthenic Syndromes, Presynaptic 		19 0 1 3.7E-04 0 0
CUI: C1969156
Disease: EEG with burst suppression
EEG with burst suppression 		19 0 1 3.7E-04 0 0
CUI: C4015465
Disease: Thoracic kyphoscoliosis
Thoracic kyphoscoliosis 		19 0 1 3.7E-04 0 0
CUI: C4023916
Disease: Aplasia/Hypoplasia of the tongue
Aplasia/Hypoplasia of the tongue 		19 0 1 3.7E-04 0 0
CUI: C4317295
Disease: Congenital disorder of glycosylation type 1s
Congenital disorder of glycosylation type 1s 		19 0 1 3.7E-04 0 0
CUI: C4551631
Disease: Cystic liver disease
Cystic liver disease 		19 0 1 3.7E-04 0 0
CUI: C0282525
Disease: Adrenoleukodystrophy, Neonatal
Adrenoleukodystrophy, Neonatal 		18 0 1 3.7E-04 0 0
CUI: C0751885
Disease: Myasthenic Syndromes, Congenital, Slow Channel
Myasthenic Syndromes, Congenital, Slow Channel 		18 0 1 3.7E-04 0 0
CUI: C1834433
Disease: Obsessive-compulsive trait
Obsessive-compulsive trait 		18 0 1 3.7E-04 0 0
CUI: C1847987
Disease: HUNTINGTON DISEASE-LIKE 2
HUNTINGTON DISEASE-LIKE 2 		18 0 1 3.7E-04 0 0