Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
LEBER CONGENITAL AMAUROSIS 3 (disorder)
0 6 0 0 4 4.3E-02
CUI: C0011053
Disease: Deafness
Deafness
23 0 1 2.0E-02 0 0
CUI: C0011991
Disease: Diarrhea
Diarrhea
9 11 1 2.8E-02 1 1.0E-02
CUI: C0013363
Disease: Dysautonomia
Dysautonomia
9 0 1 2.8E-02 0 0
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele
6 0 1 3.0E-02 0 0
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects
31 0 1 1.7E-02 0 0
CUI: C0022595
Disease: Keratosis Follicularis
Keratosis Follicularis
13 0 1 2.5E-02 0 0
CUI: C0022680
Disease: Polycystic Kidney Diseases
Polycystic Kidney Diseases
21 0 1 2.1E-02 0 0
CUI: C0024437
Disease: Macular degeneration
Macular degeneration
7 0 1 2.9E-02 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia
11 0 1 2.6E-02 0 0
CUI: C0035309
Disease: Retinal Diseases
Retinal Diseases
2 0 1 3.4E-02 0 0
CUI: C0037317
Disease: Sleep disturbances
Sleep disturbances
37 0 1 1.6E-02 0 0
CUI: C0037772
Disease: Spastic Paraplegia
Spastic Paraplegia
34 0 1 1.6E-02 0 0
CUI: C0037773
Disease: Spastic Paraplegia, Hereditary
Spastic Paraplegia, Hereditary
14 0 1 2.4E-02 0 0
CUI: C0039075
Disease: Syndactyly
Syndactyly
13 0 1 2.5E-02 0 0
CUI: C0079924
Disease: Oligohydramnios
Oligohydramnios
17 0 1 2.3E-02 0 0
CUI: C0150055
Disease: Chronic pain
Chronic pain
2 0 1 3.4E-02 0 0
CUI: C0152191
Disease: Scotoma, Central
Scotoma, Central
1 0 1 3.6E-02 0 0
CUI: C0152200
Disease: Achromatopsia
Achromatopsia
7 53 1 2.9E-02 2 1.4E-02
CUI: C0152427
Disease: Polydactyly
Polydactyly
24 0 1 2.0E-02 0 0
CUI: C0220697
Disease: POLYDACTYLY, POSTAXIAL
POLYDACTYLY, POSTAXIAL
5 0 1 3.1E-02 0 0
CUI: C0220726
Disease: Diastrophic dysplasia
Diastrophic dysplasia
13 0 1 2.5E-02 0 0
CUI: C0221357
Disease: Brachydactyly
Brachydactyly
30 0 1 1.8E-02 0 0
CUI: C0235095
Disease: Visual field constriction
Visual field constriction
1 0 1 3.6E-02 0 0
Small for gestational age (disorder)
28 0 1 1.8E-02 0 0