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: C0034882
Disease: Rectal Diseases
Rectal Diseases
1 0 1 5.3E-02 0 0
CUI: C0040422
Disease: Tonsillar Neoplasms
Tonsillar Neoplasms
1 0 1 5.3E-02 0 0
CUI: C0153618
Disease: Malignant tumor of renal pelvis
Malignant tumor of renal pelvis
1 0 1 5.3E-02 0 0
CUI: C0155563
Disease: Rheumatic mitral regurgitation
Rheumatic mitral regurgitation
1 0 1 5.3E-02 0 0
CUI: C0232308
Disease: P pulmonale by EKG (finding)
P pulmonale by EKG (finding)
1 0 1 5.3E-02 0 0
CUI: C0238293
Disease: Osteomyelosclerosis
Osteomyelosclerosis
1 0 1 5.3E-02 0 0
CUI: C0241060
Disease: Cyst of skin
Cyst of skin
1 0 1 5.3E-02 0 0
CUI: C0263583
Disease: Idiopathic guttate hypomelanosis
Idiopathic guttate hypomelanosis
1 0 1 5.3E-02 0 0
Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails
1 0 1 5.3E-02 0 0
CUI: C0333372
Disease: Abscess cavity
Abscess cavity
1 0 1 5.3E-02 0 0
CUI: C0442774
Disease: Visual acuity, no light perception
Visual acuity, no light perception
1 0 1 5.3E-02 0 0
CUI: C0456877
Disease: High grade T-cell lymphoma
High grade T-cell lymphoma
1 0 1 5.3E-02 0 0
Localized recessive dystrophic epidermolysis bullosa
1 0 1 5.3E-02 0 0
Generalized dystrophic epidermolysis bullosa
1 0 1 5.3E-02 0 0
CUI: C0748427
Disease: Right atrial enlargement
Right atrial enlargement
1 0 1 5.3E-02 0 0
Deafness, congenital onychodystrophy, recessive form
1 0 1 5.3E-02 0 0
Chronic lymphocytic leukaemia transformation
1 0 1 5.3E-02 0 0
CUI: C1300267
Disease: Brachydactyly syndrome type B
Brachydactyly syndrome type B
1 0 1 5.3E-02 0 0
CUI: C1332919
Disease: Cervical Mucinous Adenocarcinoma
Cervical Mucinous Adenocarcinoma
1 0 1 5.3E-02 0 0
CUI: C1335749
Disease: Renal Pelvis Carcinoma
Renal Pelvis Carcinoma
1 0 1 5.3E-02 0 0
CUI: C1519703
Disease: Turcot Syndrome Type 2
Turcot Syndrome Type 2
1 0 1 5.3E-02 0 0
Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp
1 0 1 5.3E-02 0 0
CUI: C1843761
Disease: TOENAIL DYSTROPHY, ISOLATED
TOENAIL DYSTROPHY, ISOLATED
1 0 1 5.3E-02 0 0
CUI: C1844529
Disease: Midclavicular aplasia
Midclavicular aplasia
1 0 1 5.3E-02 0 0
Transient bullous dermolysis of the newborn
1 0 1 5.3E-02 0 0