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: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		42 0 1 8.0E-04 0 0
CUI: C0560346
Disease: Difficulty running
Difficulty running 		38 0 1 8.0E-04 0 0
CUI: C1839603
Disease: Proximal tubulopathy
Proximal tubulopathy 		37 0 1 8.0E-04 0 0
CUI: C1720164
Disease: Central corneal thickness
Central corneal thickness 		35 0 1 8.0E-04 0 0
CUI: C0027658
Disease: Neoplasms, Germ Cell and Embryonal
Neoplasms, Germ Cell and Embryonal 		34 0 1 8.0E-04 0 0
CUI: C4228778
Disease: Abnormality of radial ray
Abnormality of radial ray 		34 0 1 8.0E-04 0 0
CUI: C4551705
Disease: Abnormality of chromosome stability
Abnormality of chromosome stability 		34 0 1 8.0E-04 0 0
CUI: C0339535
Disease: Night blindness, congenital stationary
Night blindness, congenital stationary 		32 0 1 8.0E-04 0 0
CUI: C1837066
Disease: Recurrent viral infection
Recurrent viral infection 		32 0 1 8.0E-04 0 0
CUI: C0030436
Disease: Parakeratosis
Parakeratosis 		31 0 1 8.0E-04 0 0
CUI: C1844527
Disease: Clitoral hypoplasia
Clitoral hypoplasia 		30 0 1 8.0E-04 0 0
CUI: C1855676
Disease: Aplasia/Hypoplasia of the cerebellar vermis
Aplasia/Hypoplasia of the cerebellar vermis 		30 0 1 8.0E-04 0 0
CUI: C0201973
Disease: Creatine kinase measurement
Creatine kinase measurement 		29 0 1 8.0E-04 0 0
CUI: C1850794
Disease: Proximal amyotrophy
Proximal amyotrophy 		29 0 1 8.0E-04 0 0
CUI: C0795841
Disease: Jacobsen Distal 11q Deletion Syndrome
Jacobsen Distal 11q Deletion Syndrome 		28 0 1 8.1E-04 0 0
CUI: C1843697
Disease: Axial muscle weakness
Axial muscle weakness 		28 0 1 8.1E-04 0 0
CUI: C1859126
Disease: Stippled epiphyses
Stippled epiphyses 		28 0 1 8.1E-04 0 0
CUI: C0040261
Disease: Onychomycosis
Onychomycosis 		27 0 1 8.1E-04 0 0
CUI: C0266361
Disease: True Hermaphroditism (disorder)
True Hermaphroditism (disorder) 		27 0 1 8.1E-04 0 0
CUI: C0549306
Disease: Mesomelia
Mesomelia 		27 0 1 8.1E-04 0 0
CUI: C0700225
Disease: Serum creatinine raised
Serum creatinine raised 		27 0 1 8.1E-04 0 0
CUI: C1446712
Disease: Overlapping fingers
Overlapping fingers 		27 0 1 8.1E-04 0 0
CUI: C0152200
Disease: Achromatopsia
Achromatopsia 		26 0 1 8.1E-04 0 0
CUI: C1325327
Disease: fibrinogen activity
fibrinogen activity 		26 63 1 8.1E-04 1 2.5E-03
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE 		26 63 1 8.1E-04 1 2.5E-03