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: C3853779
Disease: Neonatal Alloimmune Thrombocytopenia
Neonatal Alloimmune Thrombocytopenia 		29 0 1 8.9E-04 0 0
CUI: C0020479
Disease: Hyperlipoproteinemia Type III
Hyperlipoproteinemia Type III 		28 0 1 8.9E-04 0 0
CUI: C3158111
Disease: response to SSRI
response to SSRI 		28 0 1 8.9E-04 0 0
CUI: C1272321
Disease: Autoantibody measurement
Autoantibody measurement 		27 0 1 8.9E-04 0 0
CUI: C2749625
Disease: Motor axonal neuropathy
Motor axonal neuropathy 		27 0 1 8.9E-04 0 0
CUI: C4020730
Disease: Increased intramyocellular lipid droplets
Increased intramyocellular lipid droplets 		27 0 1 8.9E-04 0 0
CUI: C4024900
Disease: Atrophy/Degeneration affecting the brainstem
Atrophy/Degeneration affecting the brainstem 		27 0 1 8.9E-04 0 0
CUI: C0279084
Disease: Kaposi's sarcoma classical type
Kaposi's sarcoma classical type 		26 0 1 8.9E-04 0 0
CUI: C1277709
Disease: Transferrin saturation measurement
Transferrin saturation measurement 		26 0 1 8.9E-04 0 0
CUI: C1848172
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A 		26 0 1 8.9E-04 0 0
CUI: C0282528
Disease: Peroxisomal Disorders
Peroxisomal Disorders 		25 0 1 8.9E-04 0 0
CUI: C1858592
Disease: Carney Triad
Carney Triad 		25 0 1 8.9E-04 0 0
CUI: C0151564
Disease: Cogwheel Rigidity
Cogwheel Rigidity 		24 0 1 8.9E-04 0 0
CUI: C0155016
Disease: Color Blindness, Red-Green
Color Blindness, Red-Green 		24 0 1 8.9E-04 0 0
CUI: C0202231
Disease: Thyroxine measurement
Thyroxine measurement 		24 0 1 8.9E-04 0 0
CUI: C0238124
Disease: Necrotizing fasciitis
Necrotizing fasciitis 		24 0 1 8.9E-04 0 0
CUI: C0423421
Disease: Atrophic macular change
Atrophic macular change 		24 0 1 8.9E-04 0 0
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement 		23 0 1 8.9E-04 0 0
CUI: C1849140
Disease: SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE
SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE 		23 0 1 8.9E-04 0 0
CUI: C1969443
Disease: Trifunctional Protein Deficiency With Myopathy And Neuropathy
Trifunctional Protein Deficiency With Myopathy And Neuropathy 		23 0 1 8.9E-04 0 0
CUI: C0018523
Disease: Hallervorden-Spatz Syndrome
Hallervorden-Spatz Syndrome 		22 0 1 8.9E-04 0 0
CUI: C0023092
Disease: Lassa Fever
Lassa Fever 		22 0 1 8.9E-04 0 0
CUI: C0034088
Disease: Pulmonary Valve Insufficiency
Pulmonary Valve Insufficiency 		22 0 1 8.9E-04 0 0
CUI: C0035828
Disease: Romano-Ward Syndrome
Romano-Ward Syndrome 		22 0 1 8.9E-04 0 0
CUI: C1262020
Disease: Diffuse alveolar damage
Diffuse alveolar damage 		22 0 1 8.9E-04 0 0