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: C0010626
Disease: Embryonic cyst
Embryonic cyst
1 0 1 1.00 0 0
CUI: C0948779
Disease: Gastrointestinal hypomotility
Gastrointestinal hypomotility
1 0 1 1.00 0 0
CUI: C0013288
Disease: Dumping Syndrome
Dumping Syndrome
2 0 1 0.50 0 0
CUI: C2750076
Disease: Miyoshi Muscular Dystrophy 3
Miyoshi Muscular Dystrophy 3
2 0 1 0.50 0 0
CUI: C0206673
Disease: Syringoma
Syringoma
3 0 1 0.33 0 0
CUI: C0334392
Disease: Epithelial-myoepithelial carcinoma
Epithelial-myoepithelial carcinoma
3 0 1 0.33 0 0
Salivary Gland Low Grade Cribriform Cystadenocarcinoma
3 0 1 0.33 0 0
CUI: C1833736
Disease: Osteogenesis imperfecta, Levin type
Osteogenesis imperfecta, Levin type
9 0 1 0.11 0 0
CUI: C1275282
Disease: Low-grade fibromyxoid sarcoma
Low-grade fibromyxoid sarcoma
10 0 1 1.0E-01 0 0
Gastric Gastrointestinal Stromal Tumor
11 0 1 9.1E-02 0 0
Extragastrointestinal Gastrointestinal Stromal Tumor
12 0 1 8.3E-02 0 0
CUI: C0235394
Disease: Wasting
Wasting
15 0 1 6.7E-02 0 0
CUI: C0796149
Disease: Scott Syndrome
Scott Syndrome
15 0 1 6.7E-02 0 0
Mammary Analogue Secretory Carcinoma
17 0 1 5.9E-02 0 0
CUI: C0334347
Disease: Eccrine spiradenoma
Eccrine spiradenoma
20 0 1 5.0E-02 0 0
Gastroparesis with diabetes mellitus
21 0 1 4.8E-02 0 0
Polymorphous low grade adenocarcinoma
23 0 1 4.3E-02 0 0
CUI: C0152132
Disease: Hypertensive Retinopathy
Hypertensive Retinopathy
24 0 1 4.2E-02 0 0
CUI: C0006266
Disease: Bronchospasm
Bronchospasm
29 0 1 3.4E-02 0 0
CUI: C0948187
Disease: Tracheomalacia
Tracheomalacia
30 0 1 3.3E-02 0 0
CUI: C0585186
Disease: Cutaneous hypersensitivity
Cutaneous hypersensitivity
31 0 1 3.2E-02 0 0
Perivascular Epithelioid Cell Neoplasms
31 0 1 3.2E-02 0 0
CUI: C0037036
Disease: Sialorrhea
Sialorrhea
32 0 1 3.1E-02 0 0
CUI: C4543926
Disease: Narcolepsy type 1
Narcolepsy type 1
35 0 1 2.9E-02 0 0
CUI: C0003028
Disease: Anhidrosis
Anhidrosis
37 0 1 2.7E-02 0 0