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 6.2E-02 0 0
CUI: C0003516
Disease: Aortopulmonary Septal Defect
Aortopulmonary Septal Defect
1 0 1 6.2E-02 0 0
CUI: C0006386
Disease: Bunion
Bunion
1 0 1 6.2E-02 0 0
CUI: C0015231
Disease: Exanthema Subitum
Exanthema Subitum
1 0 1 6.2E-02 0 0
CUI: C0017412
Disease: Genital Diseases, Male
Genital Diseases, Male
1 0 1 6.2E-02 0 0
CUI: C0019338
Disease: Herpangina
Herpangina
1 0 1 6.2E-02 0 0
CUI: C0025469
Disease: Mesenteric Lymphadenitis
Mesenteric Lymphadenitis
1 0 1 6.2E-02 0 0
CUI: C0027095
Disease: Myosarcoma
Myosarcoma
1 0 1 6.2E-02 0 0
CUI: C0033775
Disease: Pruritus Ani
Pruritus Ani
1 0 1 6.2E-02 0 0
CUI: C0034074
Disease: Pulmonary Infarction
Pulmonary Infarction
1 0 1 6.2E-02 0 0
CUI: C0037018
Disease: Shwartzman Phenomenon
Shwartzman Phenomenon
1 0 1 6.2E-02 0 0
CUI: C0041188
Disease: Tropical pyomyositis
Tropical pyomyositis
1 0 1 6.2E-02 0 0
CUI: C0041343
Disease: Tubo-ovarian abscess
Tubo-ovarian abscess
1 0 1 6.2E-02 0 0
CUI: C0149959
Disease: Acute pelvic inflammatory disease
Acute pelvic inflammatory disease
1 0 1 6.2E-02 0 0
CUI: C0153053
Disease: Measles with complication
Measles with complication
1 0 1 6.2E-02 0 0
CUI: C0155163
Disease: Conjunctival pigmentation
Conjunctival pigmentation
1 0 1 6.2E-02 0 0
CUI: C0235014
Disease: Bulging fontanelle
Bulging fontanelle
1 0 1 6.2E-02 0 0
CUI: C0235832
Disease: Congenital hernia
Congenital hernia
1 0 1 6.2E-02 0 0
Disorder of male reproductive system
1 0 1 6.2E-02 0 0
CUI: C0262509
Disease: herpetic neuralgia
herpetic neuralgia
1 0 1 6.2E-02 0 0
CUI: C0262981
Disease: Interface dermatitis
Interface dermatitis
1 0 1 6.2E-02 0 0
CUI: C0263506
Disease: Perifolliculitis capitis abscedens
Perifolliculitis capitis abscedens
1 0 1 6.2E-02 0 0
CUI: C0263579
Disease: Pigmented hairy epidermal nevus
Pigmented hairy epidermal nevus
1 0 1 6.2E-02 0 0
CUI: C0266430
Disease: Polyorchism
Polyorchism
1 0 1 6.2E-02 0 0
CUI: C0270958
Disease: Kocher-Debre-Semelaigne syndrome
Kocher-Debre-Semelaigne syndrome
1 0 1 6.2E-02 0 0