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: C4551508
Disease: Dominant hereditary optic atrophy
Dominant hereditary optic atrophy
16 14 16 0.14 14 0.31
CUI: C0042341
Disease: Varicocele
Varicocele
99 0 20 0.10 0 0
OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY
14 22 11 9.2E-02 9 0.16
CUI: C0007868
Disease: Cervical dysplasia
Cervical dysplasia
56 0 13 8.1E-02 0 0
CUI: C0917796
Disease: Optic Atrophy, Hereditary, Leber
Optic Atrophy, Hereditary, Leber
100 46 16 8.0E-02 1 1.1E-02
CUI: C1861455
Disease: STOMATOCYTOSIS I
STOMATOCYTOSIS I
20 0 10 7.9E-02 0 0
CUI: C0268353
Disease: Cutis laxa, x-linked
Cutis laxa, x-linked
22 0 10 7.8E-02 0 0
X-linked recessive nephrolithiasis with renal failure
10 0 9 7.6E-02 0 0
CUI: C4524264
Disease: Uncomplicated pyelonephritis
Uncomplicated pyelonephritis
10 0 9 7.6E-02 0 0
CUI: C0029132
Disease: Disorder of the optic nerve
Disorder of the optic nerve
112 2 16 7.5E-02 1 2.2E-02
CUI: C4285911
Disease: C5 palsy
C5 palsy
13 0 9 7.4E-02 0 0
CUI: C0242670
Disease: Persistent Vegetative State
Persistent Vegetative State
15 0 9 7.3E-02 0 0
CUI: C3887487
Disease: Postaxial polydactyly type A
Postaxial polydactyly type A
20 0 9 7.0E-02 0 0
CUI: C0037384
Disease: Snoring
Snoring
23 0 9 6.9E-02 0 0
CUI: C0262380
Disease: Asymptomatic bacteriuria
Asymptomatic bacteriuria
23 0 9 6.9E-02 0 0
CUI: C0334276
Disease: Adenocarcinoma in Situ
Adenocarcinoma in Situ
55 0 11 6.8E-02 0 0
CUI: C0520575
Disease: Acute pyelonephritis
Acute pyelonephritis
44 0 10 6.6E-02 0 0
Cervical intraepithelial neoplasia grade 2
77 0 12 6.6E-02 0 0
CUI: C0376670
Disease: Pancreatitis, Alcoholic
Pancreatitis, Alcoholic
61 0 11 6.6E-02 0 0
CUI: C0206708
Disease: Cervical Intraepithelial Neoplasia
Cervical Intraepithelial Neoplasia
398 0 31 6.4E-02 0 0
CUI: C0853897
Disease: Diabetic Cardiomyopathies
Diabetic Cardiomyopathies
220 0 20 6.3E-02 0 0
CUI: C0034186
Disease: Pyelonephritis
Pyelonephritis
71 0 11 6.2E-02 0 0
CUI: C3825201
Disease: Mitochondrial pathology
Mitochondrial pathology
20 0 8 6.2E-02 0 0
CUI: C0751072
Disease: Frontotemporal Lobar Degeneration
Frontotemporal Lobar Degeneration
195 0 18 6.1E-02 0 0
SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE
23 0 8 6.1E-02 0 0