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: C0202071
Disease: Homovanillic acid measurement
Homovanillic acid measurement 		1 0 1 9.1E-02 0 0
CUI: C3280452
Disease: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12 		1 0 1 9.1E-02 0 0
CUI: C3825253
Disease: Cataract in old age
Cataract in old age 		1 0 1 9.1E-02 0 0
CUI: C4015519
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28 		1 0 1 9.1E-02 0 0
CUI: C4748334
Disease: DEAFNESS, AUTOSOMAL DOMINANT 74
DEAFNESS, AUTOSOMAL DOMINANT 74 		1 0 1 9.1E-02 0 0
CUI: C4749578
Disease: Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX deficiency
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX deficiency 		1 0 1 9.1E-02 0 0
CUI: C4016881
Disease: ESOPHAGEAL SQUAMOUS CELL CARCINOMA, SOMATIC
ESOPHAGEAL SQUAMOUS CELL CARCINOMA, SOMATIC 		3 0 1 7.7E-02 0 0
CUI: C1851958
Disease: Lewy Body Variant of Alzheimer Disease
Lewy Body Variant of Alzheimer Disease 		4 0 1 7.1E-02 0 0
CUI: C0153942
Disease: Benign neoplasm of esophagus
Benign neoplasm of esophagus 		6 0 1 6.2E-02 0 0
CUI: C0154059
Disease: Carcinoma in situ of esophagus
Carcinoma in situ of esophagus 		6 0 1 6.2E-02 0 0
CUI: C0399368
Disease: Amelogenesis Imperfecta, Type IB
Amelogenesis Imperfecta, Type IB 		6 0 1 6.2E-02 0 0
CUI: C3203671
Disease: CYP2D6 polymorphism
CYP2D6 polymorphism 		7 0 1 5.9E-02 0 0
CUI: C1536168
Disease: Chronic pelvic pain syndrome
Chronic pelvic pain syndrome 		8 0 1 5.6E-02 0 0
CUI: C0423319
Disease: Atrophic iris
Atrophic iris 		9 0 1 5.3E-02 0 0
CUI: C1527405
Disease: Erythrocytosis
Erythrocytosis 		9 0 1 5.3E-02 0 0
CUI: C0002351
Disease: Altitude Sickness
Altitude Sickness 		10 0 1 5.0E-02 0 0
CUI: C0743101
Disease: developmentally delayed
developmentally delayed 		11 0 1 4.8E-02 0 0
CUI: C1518716
Disease: Ovarian gonadoblastoma
Ovarian gonadoblastoma 		11 0 1 4.8E-02 0 0
CUI: C4025892
Disease: Abnormality of the labia
Abnormality of the labia 		11 0 1 4.8E-02 0 0
CUI: C4510744
Disease: 46,XY partial gonadal dysgenesis
46,XY partial gonadal dysgenesis 		11 0 1 4.8E-02 0 0
CUI: C1515283
Disease: Testicular gonadoblastoma
Testicular gonadoblastoma 		12 0 1 4.5E-02 0 0
CUI: C3463992
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1 		12 0 1 4.5E-02 0 0
CUI: C4025741
Disease: Clinodactyly of the 5th toe
Clinodactyly of the 5th toe 		13 0 1 4.3E-02 0 0
CUI: C4025895
Disease: Abnormality of the scrotum
Abnormality of the scrotum 		13 0 1 4.3E-02 0 0
CUI: C4725092
Disease: Advanced Uveal Melanoma
Advanced Uveal Melanoma 		13 0 1 4.3E-02 0 0