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: C0006262
Disease: Bronchial Fistula
Bronchial Fistula
1 0 1 7.8E-03 0 0
CUI: C0009761
Disease: Conjunctival Neoplasms
Conjunctival Neoplasms
1 0 1 7.8E-03 0 0
CUI: C0010334
Disease: Crisscross Heart
Crisscross Heart
1 0 1 7.8E-03 0 0
CUI: C0026684
Disease: Mucocele of appendix
Mucocele of appendix
1 0 1 7.8E-03 0 0
CUI: C0027645
Disease: Neoplasm Seeding
Neoplasm Seeding
1 0 1 7.8E-03 0 0
CUI: C0031557
Disease: Phlegmon
Phlegmon
1 0 1 7.8E-03 0 0
CUI: C0035290
Disease: Reticulohistiocytic granuloma
Reticulohistiocytic granuloma
1 0 1 7.8E-03 0 0
Megaloblastic anemia due to folate deficiency
1 0 1 7.8E-03 0 0
CUI: C0152091
Disease: Osteochondropathy
Osteochondropathy
1 0 1 7.8E-03 0 0
CUI: C0152190
Disease: Refractive amblyopia
Refractive amblyopia
1 0 1 7.8E-03 0 0
CUI: C0155526
Disease: Cochlear otosclerosis
Cochlear otosclerosis
1 0 1 7.8E-03 0 0
CUI: C0156353
Disease: Uterovaginal prolapse
Uterovaginal prolapse
1 0 1 7.8E-03 0 0
CUI: C0158564
Disease: Congenital vitreous anomaly
Congenital vitreous anomaly
1 0 1 7.8E-03 0 0
CUI: C0158651
Disease: Cleft lip, unilateral, complete
Cleft lip, unilateral, complete
1 0 1 7.8E-03 0 0
Congenital stenosis of pulmonary valve
1 0 1 7.8E-03 0 0
CUI: C0162504
Disease: Neutrophilic Eccrine Hidradenitis
Neutrophilic Eccrine Hidradenitis
1 0 1 7.8E-03 0 0
CUI: C0202220
Disease: Somatomedin-C measurement
Somatomedin-C measurement
1 0 1 7.8E-03 0 0
CUI: C0232259
Disease: Mid-systolic murmur
Mid-systolic murmur
1 0 1 7.8E-03 0 0
CUI: C0232288
Disease: Chest pain on exertion
Chest pain on exertion
1 0 1 7.8E-03 0 0
CUI: C0233286
Disease: Frank Breech Presentation
Frank Breech Presentation
1 1 1 7.8E-03 1 1.0E-01
CUI: C0237932
Disease: emotional trauma
emotional trauma
1 0 1 7.8E-03 0 0
CUI: C0239894
Disease: HEART DISPLACEMENT
HEART DISPLACEMENT
1 0 1 7.8E-03 0 0
CUI: C0241633
Disease: Vaginal dryness
Vaginal dryness
1 0 1 7.8E-03 0 0
CUI: C0242012
Disease: NEPHROTIC SYNDROME, CHRONIC
NEPHROTIC SYNDROME, CHRONIC
1 0 1 7.8E-03 0 0
CUI: C0243057
Disease: Stomatognathic System Abnormalities
Stomatognathic System Abnormalities
1 0 1 7.8E-03 0 0