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: C0585475
Disease: Pilomatrix carcinoma of skin
Pilomatrix carcinoma of skin
0 3 0 0 3 2.6E-02
CUI: C1167918
Disease: Increased CSF lactate
Increased CSF lactate
87 0 1 1.1E-03 0 0
CUI: C0202202
Disease: Protein measurement
Protein measurement
75 0 1 1.1E-03 0 0
CUI: C0919677
Disease: Protein C measurement
Protein C measurement
62 0 1 1.1E-03 0 0
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement
62 0 1 1.1E-03 0 0
CUI: C0751401
Disease: Ophthalmoparesis
Ophthalmoparesis
61 0 1 1.1E-03 0 0
Fatigable weakness of respiratory muscles
60 0 1 1.1E-03 0 0
CUI: C0232744
Disease: Decreased liver function
Decreased liver function
59 0 1 1.1E-03 0 0
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
58 0 1 1.1E-03 0 0
CUI: C0235095
Disease: Visual field constriction
Visual field constriction
57 0 1 1.1E-03 0 0
CUI: C1306620
Disease: Systolic blood pressure measurement
Systolic blood pressure measurement
54 0 1 1.1E-03 0 0
CUI: C0337443
Disease: Sodium measurement
Sodium measurement
53 0 1 1.1E-03 0 0
CUI: C0426789
Disease: Short thorax
Short thorax
51 0 1 1.1E-03 0 0
CUI: C0018520
Disease: Halitosis
Halitosis
48 0 1 1.1E-03 0 0
CUI: C0271385
Disease: Horizontal Nystagmus
Horizontal Nystagmus
48 0 1 1.1E-03 0 0
CUI: C0730290
Disease: Cone Dystrophy
Cone Dystrophy
48 0 1 1.1E-03 0 0
CUI: C0001916
Disease: Albinism
Albinism
46 0 1 1.1E-03 0 0
CUI: C0344530
Disease: Congenital keratoglobus
Congenital keratoglobus
46 0 1 1.1E-03 0 0
CUI: C0376532
Disease: Epilepsy, Rolandic
Epilepsy, Rolandic
46 0 1 1.1E-03 0 0
CUI: C1849488
Disease: Increased serum pyruvate
Increased serum pyruvate
45 0 1 1.1E-03 0 0
CUI: C2112129
Disease: Postaxial foot polydactyly
Postaxial foot polydactyly
45 0 1 1.1E-03 0 0
CUI: C0427055
Disease: Facial Paresis
Facial Paresis
44 0 1 1.1E-03 0 0
CUI: C1271100
Disease: Lower limb spasticity
Lower limb spasticity
43 0 1 1.1E-03 0 0
CUI: C0272242
Disease: Complement deficiency disease
Complement deficiency disease
42 0 1 1.1E-03 0 0
CUI: C1836003
Disease: Facial diplegia
Facial diplegia
42 0 1 1.1E-03 0 0