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: C0027333
Disease: Nagana
Nagana 		10 0 1 7.7E-02 0 0
CUI: C0025637
Disease: Methemoglobinemia
Methemoglobinemia 		12 0 1 6.7E-02 0 0
CUI: C0206307
Disease: Canavan Disease
Canavan Disease 		12 0 1 6.7E-02 0 0
CUI: C0268059
Disease: Neonatal hemochromatosis
Neonatal hemochromatosis 		13 0 1 6.2E-02 0 0
CUI: C0221333
Disease: Hypouricemia
Hypouricemia 		14 0 1 5.9E-02 0 0
CUI: C2732979
Disease: Acquired long QT syndrome
Acquired long QT syndrome 		14 0 1 5.9E-02 0 0
CUI: C3276549
Disease: OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY
OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY 		14 0 1 5.9E-02 0 0
CUI: C2713442
Disease: Polyposis, Adenomatous Intestinal
Polyposis, Adenomatous Intestinal 		16 0 1 5.3E-02 0 0
CUI: C2713443
Disease: Familial Intestinal Polyposis
Familial Intestinal Polyposis 		16 0 1 5.3E-02 0 0
CUI: C1855681
Disease: Nephronophthisis, familial juvenile
Nephronophthisis, familial juvenile 		17 0 1 5.0E-02 0 0
CUI: C0848771
Disease: neurological disability
neurological disability 		18 0 1 4.8E-02 0 0
CUI: C3494489
Disease: Autoimmune polyendocrinopathy syndrome, type 1
Autoimmune polyendocrinopathy syndrome, type 1 		18 0 1 4.8E-02 0 0
CUI: C4551979
Disease: Nephronophthisis 1
Nephronophthisis 1 		18 0 1 4.8E-02 0 0
CUI: C0678128
Disease: Friend leukemia
Friend leukemia 		19 0 1 4.5E-02 0 0
CUI: C0002514
Disease: Amino Acid Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors 		20 0 1 4.3E-02 0 0
CUI: C2931672
Disease: Cerebral hemorrhage with amyloidosis, hereditary, Dutch type
Cerebral hemorrhage with amyloidosis, hereditary, Dutch type 		20 0 1 4.3E-02 0 0
CUI: C0009946
Disease: Conversion disorder
Conversion disorder 		21 0 1 4.2E-02 0 0
CUI: C0342783
Disease: Deficiency of butyryl-CoA dehydrogenase
Deficiency of butyryl-CoA dehydrogenase 		21 0 1 4.2E-02 0 0
CUI: C0751689
Disease: Peripheral Nerve Sheath Neoplasm
Peripheral Nerve Sheath Neoplasm 		22 0 1 4.0E-02 0 0
CUI: C0085625
Disease: Hypoalgesia
Hypoalgesia 		23 0 1 3.8E-02 0 0
CUI: C0393814
Disease: Hereditary liability to pressure palsies
Hereditary liability to pressure palsies 		23 0 1 3.8E-02 0 0
CUI: C0406709
Disease: Hay-Wells syndrome
Hay-Wells syndrome 		26 0 1 3.4E-02 0 0
CUI: C0020479
Disease: Hyperlipoproteinemia Type III
Hyperlipoproteinemia Type III 		28 0 1 3.2E-02 0 0
CUI: C0205711
Disease: Pelizaeus-Merzbacher Disease
Pelizaeus-Merzbacher Disease 		30 0 1 3.0E-02 0 0
CUI: C0039292
Disease: Tangier Disease
Tangier Disease 		31 0 1 2.9E-02 0 0