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: C0029927
Disease: Ovarian Cysts
Ovarian Cysts 		74 0 36 0.49 0 0
CUI: C1859682
Disease: Hypoplastic frontal sinuses
Hypoplastic frontal sinuses 		7 0 2 4.9E-02 0 0
CUI: C2936665
Disease: Immunoglobulin Deficiency, Late-Onset
Immunoglobulin Deficiency, Late-Onset 		11 0 2 4.4E-02 0 0
CUI: C1848389
Disease: Posterior pharyngeal cleft
Posterior pharyngeal cleft 		12 0 2 4.3E-02 0 0
CUI: C0003257
Disease: Antibody Deficiency Syndrome
Antibody Deficiency Syndrome 		21 0 2 3.6E-02 0 0
CUI: C0345375
Disease: Congenital hypoplasia of femur
Congenital hypoplasia of femur 		22 0 2 3.6E-02 0 0
CUI: C1850900
Disease: Familial primary gastric lymphoma
Familial primary gastric lymphoma 		121 0 5 3.3E-02 0 0
CUI: C1858452
Disease: Thickened calvaria
Thickened calvaria 		27 0 2 3.3E-02 0 0
CUI: C0157946
Disease: Osteoarthrosis, localized, not specified whether primary or secondary
Osteoarthrosis, localized, not specified whether primary or secondary 		28 0 2 3.2E-02 0 0
CUI: C0038015
Disease: Spondyloepiphyseal Dysplasia
Spondyloepiphyseal Dysplasia 		29 0 2 3.2E-02 0 0
CUI: C0741796
Disease: Recurrent bronchitis
Recurrent bronchitis 		29 0 2 3.2E-02 0 0
CUI: C1866134
Disease: Wide anterior fontanel
Wide anterior fontanel 		71 0 3 2.9E-02 0 0
CUI: C0002453
Disease: Amenorrhea
Amenorrhea 		37 0 2 2.8E-02 0 0
CUI: C0021361
Disease: Female infertility
Female infertility 		37 0 2 2.8E-02 0 0
CUI: C0432211
Disease: Spondyloepimetaphyseal disorder
Spondyloepimetaphyseal disorder 		37 0 2 2.8E-02 0 0
CUI: C2900450
Disease: Other Creutzfeldt-Jakob disease
Other Creutzfeldt-Jakob disease 		37 0 2 2.8E-02 0 0
CUI: C0016724
Disease: Froehlich's Syndrome
Froehlich's Syndrome 		1 0 1 2.8E-02 0 0
CUI: C0025048
Disease: Meconium Aspiration Syndrome
Meconium Aspiration Syndrome 		38 0 2 2.8E-02 0 0
CUI: C0026683
Disease: Mucocele
Mucocele 		1 0 1 2.8E-02 0 0
CUI: C0035354
Disease: Retrograde Degeneration
Retrograde Degeneration 		1 0 1 2.8E-02 0 0
CUI: C0266572
Disease: Congenital anomaly of eyelid
Congenital anomaly of eyelid 		1 0 1 2.8E-02 0 0
CUI: C0398764
Disease: Complement Factor D Deficiency
Complement Factor D Deficiency 		1 0 1 2.8E-02 0 0
CUI: C0575827
Disease: Small finger
Small finger 		1 0 1 2.8E-02 0 0
CUI: C0751505
Disease: Insufficient Sleep Syndrome
Insufficient Sleep Syndrome 		1 0 1 2.8E-02 0 0
CUI: C0751507
Disease: Sleep Fragmentation
Sleep Fragmentation 		1 0 1 2.8E-02 0 0