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: C0005911
Disease: Body Weight Changes
Body Weight Changes 		1 0 1 3.1E-02 0 0
CUI: C0016697
Disease: Freemartinism
Freemartinism 		1 0 1 3.1E-02 0 0
CUI: C0018944
Disease: Hematoma
Hematoma 		1 0 1 3.1E-02 0 0
CUI: C0151482
Disease: Megaloblastic anemia due to folate deficiency
Megaloblastic anemia due to folate deficiency 		1 0 1 3.1E-02 0 0
CUI: C0152072
Disease: Ovale malaria
Ovale malaria 		1 0 1 3.1E-02 0 0
CUI: C0202220
Disease: Somatomedin-C measurement
Somatomedin-C measurement 		1 0 1 3.1E-02 0 0
CUI: C0238110
Disease: Chronic epididymitis
Chronic epididymitis 		1 0 1 3.1E-02 0 0
CUI: C0242012
Disease: NEPHROTIC SYNDROME, CHRONIC
NEPHROTIC SYNDROME, CHRONIC 		1 0 1 3.1E-02 0 0
CUI: C0267494
Disease: Chilaiditi Syndrome
Chilaiditi Syndrome 		1 0 1 3.1E-02 0 0
CUI: C0267896
Disease: Mucocele of gallbladder
Mucocele of gallbladder 		1 0 1 3.1E-02 0 0
CUI: C0268152
Disease: Classical galactosemia, homozygous Duarte-type
Classical galactosemia, homozygous Duarte-type 		1 1 1 3.1E-02 1 4.3E-03
CUI: C0268461
Disease: Disorder of phenylalanine metabolism
Disorder of phenylalanine metabolism 		1 0 1 3.1E-02 0 0
CUI: C0271149
Disease: Secondary angle-closure glaucoma
Secondary angle-closure glaucoma 		1 0 1 3.1E-02 0 0
CUI: C0271152
Disease: Malignant glaucoma
Malignant glaucoma 		1 0 1 3.1E-02 0 0
CUI: C0271629
Disease: Mullerian inhibiting factor deficiency
Mullerian inhibiting factor deficiency 		1 0 1 3.1E-02 0 0
CUI: C0271905
Disease: Acquired methemoglobinemia
Acquired methemoglobinemia 		1 0 1 3.1E-02 0 0
CUI: C0272132
Disease: Drug-induced hemolytic anemia
Drug-induced hemolytic anemia 		1 0 1 3.1E-02 0 0
CUI: C0272405
Disease: Functional asplenia
Functional asplenia 		1 0 1 3.1E-02 0 0
CUI: C0300934
Disease: Primary Amebic Meningoencephalitis
Primary Amebic Meningoencephalitis 		1 0 1 3.1E-02 0 0
CUI: C0339678
Disease: Simple myopia
Simple myopia 		1 0 1 3.1E-02 0 0
CUI: C0339697
Disease: Congenital color blindness
Congenital color blindness 		1 0 1 3.1E-02 0 0
CUI: C0339916
Disease: Viral upper respiratory tract infection
Viral upper respiratory tract infection 		1 0 1 3.1E-02 0 0
CUI: C0341037
Disease: Lateral developmental cyst of jaw
Lateral developmental cyst of jaw 		1 0 1 3.1E-02 0 0
CUI: C0342745
Disease: Disorder of galactose metabolism
Disorder of galactose metabolism 		1 0 1 3.1E-02 0 0
CUI: C0404562
Disease: Incipient ovarian failure
Incipient ovarian failure 		1 0 1 3.1E-02 0 0