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: C0002797
Disease: Bovine Anaplasmosis
Bovine Anaplasmosis
1 0 1 6.7E-02 0 0
CUI: C0006386
Disease: Bunion
Bunion
1 0 1 6.7E-02 0 0
CUI: C0008522
Disease: Choroid Hemorrhage
Choroid Hemorrhage
1 0 1 6.7E-02 0 0
CUI: C0014127
Disease: Endocervicitis
Endocervicitis
1 0 1 6.7E-02 0 0
CUI: C0027095
Disease: Myosarcoma
Myosarcoma
1 0 1 6.7E-02 0 0
CUI: C0037018
Disease: Shwartzman Phenomenon
Shwartzman Phenomenon
1 0 1 6.7E-02 0 0
CUI: C0152091
Disease: Osteochondropathy
Osteochondropathy
1 0 1 6.7E-02 0 0
CUI: C0153053
Disease: Measles with complication
Measles with complication
1 0 1 6.7E-02 0 0
CUI: C0156353
Disease: Uterovaginal prolapse
Uterovaginal prolapse
1 0 1 6.7E-02 0 0
CUI: C0158763
Disease: Macrodactylia of fingers
Macrodactylia of fingers
1 0 1 6.7E-02 0 0
CUI: C0158768
Disease: Macrodactyly of toe
Macrodactyly of toe
1 0 1 6.7E-02 0 0
CUI: C0158784
Disease: Accessory skeletal muscle
Accessory skeletal muscle
1 0 1 6.7E-02 0 0
CUI: C0262509
Disease: herpetic neuralgia
herpetic neuralgia
1 0 1 6.7E-02 0 0
CUI: C0262981
Disease: Interface dermatitis
Interface dermatitis
1 0 1 6.7E-02 0 0
CUI: C0263506
Disease: Perifolliculitis capitis abscedens
Perifolliculitis capitis abscedens
1 0 1 6.7E-02 0 0
CUI: C0268417
Disease: Pancreatic trypsinogen deficiency
Pancreatic trypsinogen deficiency
1 0 1 6.7E-02 0 0
Yellow mutant oculocutaneous albinism
1 0 1 6.7E-02 0 0
CUI: C0275974
Disease: Glandular tularemia
Glandular tularemia
1 0 1 6.7E-02 0 0
CUI: C0276379
Disease: La Crosse Encephalitis
La Crosse Encephalitis
1 0 1 6.7E-02 0 0
recurrent Wilms tumor and other childhood kidney tumors
1 0 1 6.7E-02 0 0
lip and oral cavity squamous cell carcinoma
1 0 1 6.7E-02 0 0
CUI: C0333008
Disease: Congenital hypopigmentation
Congenital hypopigmentation
1 0 1 6.7E-02 0 0
CUI: C0339317
Disease: Non-infectious anterior uveitis
Non-infectious anterior uveitis
1 0 1 6.7E-02 0 0
Granulomatous interstitial nephritis
1 0 1 6.7E-02 0 0
CUI: C0342683
Disease: ALBINISM, OCULOCUTANEOUS, TYPE III
ALBINISM, OCULOCUTANEOUS, TYPE III
1 0 1 6.7E-02 0 0