Source: ALL
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: C0015231
Disease: Exanthema Subitum
Exanthema Subitum 		1 0 1 5.6E-02 0 0
CUI: C0019338
Disease: Herpangina
Herpangina 		1 0 1 5.6E-02 0 0
CUI: C0021295
Disease: Infant, Premature, Diseases
Infant, Premature, Diseases 		1 0 1 5.6E-02 0 0
CUI: C0025469
Disease: Mesenteric Lymphadenitis
Mesenteric Lymphadenitis 		1 0 1 5.6E-02 0 0
CUI: C0029804
Disease: Other specified hemorrhagic conditions
Other specified hemorrhagic conditions 		1 0 1 5.6E-02 0 0
CUI: C0029942
Disease: Overanxious disorder
Overanxious disorder 		1 0 1 5.6E-02 0 0
CUI: C0033775
Disease: Pruritus Ani
Pruritus Ani 		1 0 1 5.6E-02 0 0
CUI: C0034074
Disease: Pulmonary Infarction
Pulmonary Infarction 		1 0 1 5.6E-02 0 0
CUI: C0041188
Disease: Tropical pyomyositis
Tropical pyomyositis 		1 0 1 5.6E-02 0 0
CUI: C0041343
Disease: Tubo-ovarian abscess
Tubo-ovarian abscess 		1 0 1 5.6E-02 0 0
CUI: C0085128
Disease: Cardiac Output, High
Cardiac Output, High 		1 0 1 5.6E-02 0 0
CUI: C0149959
Disease: Acute pelvic inflammatory disease
Acute pelvic inflammatory disease 		1 0 1 5.6E-02 0 0
CUI: C0178426
Disease: Oligohydramnios sequence
Oligohydramnios sequence 		1 0 1 5.6E-02 0 0
CUI: C0235014
Disease: Bulging fontanelle
Bulging fontanelle 		1 0 1 5.6E-02 0 0
CUI: C0240211
Disease: Lip swelling
Lip swelling 		1 0 1 5.6E-02 0 0
CUI: C0242875
Disease: Ventricular Septal Rupture
Ventricular Septal Rupture 		1 0 1 5.6E-02 0 0
CUI: C0263478
Disease: Ophiasis
Ophiasis 		1 0 1 5.6E-02 0 0
CUI: C0264487
Disease: Chronic nonspecific lung disease
Chronic nonspecific lung disease 		1 0 1 5.6E-02 0 0
CUI: C0272195
Disease: Eosinopenia
Eosinopenia 		1 0 1 5.6E-02 0 0
CUI: C0272383
Disease: Suppurative tonsillitis
Suppurative tonsillitis 		1 0 1 5.6E-02 0 0
CUI: C0339882
Disease: Laryngeal amyloidosis
Laryngeal amyloidosis 		1 0 1 5.6E-02 0 0
CUI: C0340535
Disease: Acute massive pulmonary embolism
Acute massive pulmonary embolism 		1 0 1 5.6E-02 0 0
CUI: C0340804
Disease: Hereditary vascular fragility
Hereditary vascular fragility 		1 0 1 5.6E-02 0 0
CUI: C0341117
Disease: Esophageal erosions
Esophageal erosions 		1 0 1 5.6E-02 0 0
CUI: C0342266
Disease: Insulin treated type 2 diabetes mellitus
Insulin treated type 2 diabetes mellitus 		1 0 1 5.6E-02 0 0