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: C0442840
Disease: Cardiac embolism
Cardiac embolism 		1 0 1 8.3E-02 0 0
CUI: C2746083
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 77 (disorder)
DEAFNESS, AUTOSOMAL RECESSIVE 77 (disorder) 		1 0 1 8.3E-02 0 0
CUI: C3281153
Disease: EFAVIRENZ, POOR METABOLISM OF
EFAVIRENZ, POOR METABOLISM OF 		1 0 1 8.3E-02 0 0
CUI: C0233767
Disease: Hallucinations, Tactile
Hallucinations, Tactile 		2 0 1 7.7E-02 0 0
CUI: C1858142
Disease: ICHTHYOSIS, LAMELLAR, 3
ICHTHYOSIS, LAMELLAR, 3 		2 0 1 7.7E-02 0 0
CUI: C3665815
Disease: CYP2B6 polymorphism
CYP2B6 polymorphism 		2 0 1 7.7E-02 0 0
CUI: C0523459
Disease: Alanine measurement
Alanine measurement 		3 0 1 7.1E-02 0 0
CUI: C2985175
Disease: Extraventricular neurocytoma
Extraventricular neurocytoma 		3 0 1 7.1E-02 0 0
CUI: C3888513
Disease: CYP2C9 polymorphism
CYP2C9 polymorphism 		3 0 1 7.1E-02 0 0
CUI: C0235942
Disease: Abnormality of the skull
Abnormality of the skull 		4 0 1 6.7E-02 0 0
CUI: C0268293
Disease: Corticosterone Methyl Oxidase Type I Deficiency
Corticosterone Methyl Oxidase Type I Deficiency 		4 0 1 6.7E-02 0 0
CUI: C0271725
Disease: Iatrogenic Cushing's disease
Iatrogenic Cushing's disease 		4 0 1 6.7E-02 0 0
CUI: C0751572
Disease: Vertebrobasilar Dolichoectasia
Vertebrobasilar Dolichoectasia 		4 0 1 6.7E-02 0 0
CUI: C3463917
Disease: Corticosterone Methyl Oxidase Type II Deficiency
Corticosterone Methyl Oxidase Type II Deficiency 		4 0 1 6.7E-02 0 0
CUI: C0221199
Disease: Abnormal palmar creases
Abnormal palmar creases 		5 0 1 6.2E-02 0 0
CUI: C0271528
Disease: Isosexual precocious puberty
Isosexual precocious puberty 		5 0 1 6.2E-02 0 0
CUI: C0342474
Disease: Lipoid congenital adrenal hyperplasia
Lipoid congenital adrenal hyperplasia 		5 0 1 6.2E-02 0 0
CUI: C1291245
Disease: Cortisone reductase deficiency
Cortisone reductase deficiency 		5 0 1 6.2E-02 0 0
CUI: C3548532
Disease: response to alcohol
response to alcohol 		5 0 1 6.2E-02 0 0
CUI: C0268689
Disease: Vitamin D-dependent rickets, type 1
Vitamin D-dependent rickets, type 1 		6 0 1 5.9E-02 0 0
CUI: C1533041
Disease: Primary congenital glaucoma
Primary congenital glaucoma 		24 0 2 5.9E-02 0 0
CUI: C1857800
Disease: CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 2
CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 2 		6 0 1 5.9E-02 0 0
CUI: C1860042
Disease: Antley-Bixler Syndrome with Disordered Steroidogenesis
Antley-Bixler Syndrome with Disordered Steroidogenesis 		6 0 1 5.9E-02 0 0
CUI: C1960539
Disease: Aromatase deficiency
Aromatase deficiency 		6 0 1 5.9E-02 0 0
CUI: C4015779
Disease: PROSTATE CANCER, SOMATIC
PROSTATE CANCER, SOMATIC 		6 0 1 5.9E-02 0 0