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: C0027645
Disease: Neoplasm Seeding
Neoplasm Seeding
1 0 1 4.2E-02 0 0
CUI: C0149640
Disease: Cecum Carcinoma
Cecum Carcinoma
1 0 1 4.2E-02 0 0
CUI: C0393602
Disease: Isolated cervical dystonia
Isolated cervical dystonia
1 0 1 4.2E-02 0 0
Other chronic tubulo-interstitial nephritis
1 0 1 4.2E-02 0 0
Neurofibromatosis 1 and 2 (NF1 and NF2)
1 0 1 4.2E-02 0 0
CUI: C0677861
Disease: Bilateral Malignant Neoplasm
Bilateral Malignant Neoplasm
1 0 1 4.2E-02 0 0
Idiopathic polypoidal choroidal vasculopathy
1 0 1 4.2E-02 0 0
CUI: C0751588
Disease: Benign Supratentorial Neoplasms
Benign Supratentorial Neoplasms
1 0 1 4.2E-02 0 0
CUI: C0751589
Disease: Cancer, Supratentorial
Cancer, Supratentorial
1 0 1 4.2E-02 0 0
CUI: C0751590
Disease: Primary Supratentorial Neoplasms
Primary Supratentorial Neoplasms
1 0 1 4.2E-02 0 0
Nonobstructive chronic pyelonephritis NOS
1 0 1 4.2E-02 0 0
CUI: C1711192
Disease: Sporadic Gastric Adenocarcinoma
Sporadic Gastric Adenocarcinoma
1 0 1 4.2E-02 0 0
CUI: C1836482
Disease: Li-Fraumeni Syndrome 2
Li-Fraumeni Syndrome 2
1 0 1 4.2E-02 0 0
T-CELL PROLYMPHOCYTIC LEUKEMIA, SOMATIC
1 0 1 4.2E-02 0 0
CUI: C1846529
Disease: CONE-ROD DYSTROPHY 10
CONE-ROD DYSTROPHY 10
1 0 1 4.2E-02 0 0
CUI: C1851057
Disease: Normal motor development
Normal motor development
1 0 1 4.2E-02 0 0
CUI: C1853214
Disease: RETINITIS PIGMENTOSA 35
RETINITIS PIGMENTOSA 35
1 0 1 4.2E-02 0 0
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 7 (disorder)
1 0 1 4.2E-02 0 0
BREAST AND COLORECTAL CANCER, SUSCEPTIBILITY TO
1 0 1 4.2E-02 0 0
CANCER OF MULTIPLE TYPES, SUSCEPTIBILITY TO
1 0 1 4.2E-02 0 0
CUI: C1859624
Disease: Defective B cell differentiation
Defective B cell differentiation
1 0 1 4.2E-02 0 0
CUI: C2033037
Disease: Pancreatic Vipoma
Pancreatic Vipoma
1 0 1 4.2E-02 0 0
Triple-Negative Breast Cancer Finding
1 0 1 4.2E-02 0 0
B Lymphoblastic Leukemia/Lymphoma, Not Otherwise Specified
1 0 1 4.2E-02 0 0
Rhabdoid Tumor Predisposition Syndrome 2
1 0 1 4.2E-02 0 0