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: C0154017
Disease: Benign neoplasm of bladder
Benign neoplasm of bladder
15 0 15 1.00 0 0
CUI: C0154091
Disease: Carcinoma in situ of bladder
Carcinoma in situ of bladder
16 0 15 0.94 0 0
Focal Cortical Dysplasia of Taylor, Type IIa
3 0 2 0.12 0 0
Focal Cortical Dysplasia of Taylor, Type IIb
3 0 2 0.12 0 0
CUI: C3278024
Disease: Enlarged cerebellum
Enlarged cerebellum
3 0 2 0.12 0 0
CUI: C0334443
Disease: Epithelioid Cell Melanoma
Epithelioid Cell Melanoma
4 0 2 0.12 0 0
Nevus, Keratinocytic, Nonepidermolytic
4 0 2 0.12 0 0
CUI: C3179502
Disease: Linear Verrucous Epidermal Nevus
Linear Verrucous Epidermal Nevus
5 0 2 0.11 0 0
CUI: C0362030
Disease: Verrucous epidermal nevus
Verrucous epidermal nevus
6 0 2 0.11 0 0
CUI: C0406803
Disease: Syringocystadenoma Papilliferum
Syringocystadenoma Papilliferum
6 0 2 0.11 0 0
Multifocal micronodular pneumocyte hyperplasia
6 0 2 0.11 0 0
Papillary renal cell carcinoma, sporadic
17 0 3 0.10 0 0
CUI: C0265329
Disease: Organoid Nevus Phakomatosis
Organoid Nevus Phakomatosis
7 0 2 1.0E-01 0 0
Papillary transitional cell neoplasm of low malignant potential
7 0 2 1.0E-01 0 0
CUI: C4725076
Disease: Advanced Urothelial Carcinoma
Advanced Urothelial Carcinoma
18 0 3 1.0E-01 0 0
CUI: C1857953
Disease: Deep plantar creases
Deep plantar creases
19 0 3 9.7E-02 0 0
CUI: C1849677
Disease: Numerous nevi
Numerous nevi
8 0 2 9.5E-02 0 0
CUI: C4478701
Disease: Focal cortical dysplasia type IIb
Focal cortical dysplasia type IIb
8 0 2 9.5E-02 0 0
CUI: C0334517
Disease: Spermatocytic seminoma
Spermatocytic seminoma
9 0 2 9.1E-02 0 0
CUI: C1335473
Disease: Primary chondrosarcoma of bone
Primary chondrosarcoma of bone
10 0 2 8.7E-02 0 0
CUI: C1857539
Disease: Deep palmar crease
Deep palmar crease
23 0 3 8.6E-02 0 0
CUI: C0039743
Disease: Thanatophoric Dysplasia
Thanatophoric Dysplasia
12 0 2 8.0E-02 0 0
CUI: C0349649
Disease: Pulmonary lymphangioleiomyomatosis
Pulmonary lymphangioleiomyomatosis
12 0 2 8.0E-02 0 0
CUI: C0751483
Disease: Familial Retinoblastoma
Familial Retinoblastoma
12 0 2 8.0E-02 0 0
CUI: C4531138
Disease: Short telomere length
Short telomere length
12 0 2 8.0E-02 0 0