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: C0268140
Disease: Xeroderma pigmentosum, group F
Xeroderma pigmentosum, group F 		0 31 0 0 3 5.8E-02
CUI: C1167918
Disease: Increased CSF lactate
Increased CSF lactate 		87 0 1 1.2E-03 0 0
CUI: C1847584
Disease: Distal sensory impairment
Distal sensory impairment 		86 0 1 1.2E-03 0 0
CUI: C0202202
Disease: Protein measurement
Protein measurement 		75 0 1 1.2E-03 0 0
CUI: C1314665
Disease: Serum alkaline phosphatase raised
Serum alkaline phosphatase raised 		67 0 1 1.2E-03 0 0
CUI: C0919677
Disease: Protein C measurement
Protein C measurement 		62 0 1 1.2E-03 0 0
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement 		62 0 1 1.2E-03 0 0
CUI: C0751401
Disease: Ophthalmoparesis
Ophthalmoparesis 		61 0 1 1.2E-03 0 0
CUI: C3277226
Disease: Restrictive ventilatory defect
Restrictive ventilatory defect 		61 0 1 1.2E-03 0 0
CUI: C4022587
Disease: Fatigable weakness of respiratory muscles
Fatigable weakness of respiratory muscles 		60 0 1 1.2E-03 0 0
CUI: C0232744
Disease: Decreased liver function
Decreased liver function 		59 0 1 1.2E-03 0 0
CUI: C0235095
Disease: Visual field constriction
Visual field constriction 		57 0 1 1.2E-03 0 0
CUI: C1836150
Disease: Gait imbalance
Gait imbalance 		57 0 1 1.2E-03 0 0
CUI: C0151849
Disease: Alkaline phosphatase raised
Alkaline phosphatase raised 		55 0 1 1.2E-03 0 0
CUI: C1306620
Disease: Systolic blood pressure measurement
Systolic blood pressure measurement 		54 0 1 1.2E-03 0 0
CUI: C0337443
Disease: Sodium measurement
Sodium measurement 		53 0 1 1.2E-03 0 0
CUI: C0426789
Disease: Short thorax
Short thorax 		51 0 1 1.2E-03 0 0
CUI: C1865037
Disease: Cone-shaped epiphysis
Cone-shaped epiphysis 		49 0 1 1.2E-03 0 0
CUI: C0018520
Disease: Halitosis
Halitosis 		48 0 1 1.2E-03 0 0
CUI: C0271385
Disease: Horizontal Nystagmus
Horizontal Nystagmus 		48 0 1 1.2E-03 0 0
CUI: C0730290
Disease: Cone Dystrophy
Cone Dystrophy 		48 0 1 1.2E-03 0 0
CUI: C0001916
Disease: Albinism
Albinism 		46 0 1 1.2E-03 0 0
CUI: C0344530
Disease: Congenital keratoglobus
Congenital keratoglobus 		46 0 1 1.2E-03 0 0
CUI: C0376532
Disease: Epilepsy, Rolandic
Epilepsy, Rolandic 		46 0 1 1.2E-03 0 0
CUI: C1136179
Disease: Hammer Toe
Hammer Toe 		46 0 1 1.2E-03 0 0