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: C1836843
Disease: Progressive inability to walk
Progressive inability to walk 		10 0 1 1.5E-04 0 0
CUI: C2348199
Disease: Short Qt Syndrome
Short Qt Syndrome 		10 0 1 1.5E-04 0 0
CUI: C3552099
Disease: Respiratory insufficiency due to defective ciliary clearance
Respiratory insufficiency due to defective ciliary clearance 		10 0 1 1.5E-04 0 0
CUI: C3806442
Disease: Myoclonic spasms
Myoclonic spasms 		10 0 1 1.5E-04 0 0
CUI: C4015098
Disease: Hypoglycosylation of alpha-dystroglycan
Hypoglycosylation of alpha-dystroglycan 		10 0 1 1.5E-04 0 0
CUI: C4022646
Disease: Reduced muscle fiber alpha dystroglycan
Reduced muscle fiber alpha dystroglycan 		10 0 1 1.5E-04 0 0
CUI: C4025360
Disease: Functional motor deficit
Functional motor deficit 		10 0 1 1.5E-04 0 0
CUI: C4072908
Disease: Induced vaginal delivery
Induced vaginal delivery 		10 0 1 1.5E-04 0 0
CUI: C0002623
Disease: Post-traumatic amnesia
Post-traumatic amnesia 		9 0 1 1.5E-04 0 0
CUI: C0015190
Disease: Euthyroid Sick Syndromes
Euthyroid Sick Syndromes 		9 0 1 1.5E-04 0 0
CUI: C0155015
Disease: Color Blindness, Red
Color Blindness, Red 		9 0 1 1.5E-04 0 0
CUI: C0239941
Disease: Persistence of hemoglobin F
Persistence of hemoglobin F 		9 0 1 1.5E-04 0 0
CUI: C0270210
Disease: Lucey-Driscoll syndrome (disorder)
Lucey-Driscoll syndrome (disorder) 		9 0 1 1.5E-04 0 0
CUI: C0393598
Disease: Idiopathic familial dystonia
Idiopathic familial dystonia 		9 0 1 1.5E-04 0 0
CUI: C0751267
Disease: Encephalopathy, Subacute Necrotizing, Infantile
Encephalopathy, Subacute Necrotizing, Infantile 		9 0 1 1.5E-04 0 0
CUI: C0751268
Disease: Encephalopathy, Subacute Necrotizing, Juvenile
Encephalopathy, Subacute Necrotizing, Juvenile 		9 0 1 1.5E-04 0 0
CUI: C0853085
Disease: Decreased LDL cholesterol concentration
Decreased LDL cholesterol concentration 		9 0 1 1.5E-04 0 0
CUI: C1852534
Disease: Hypoplastic male external genitalia
Hypoplastic male external genitalia 		9 0 1 1.5E-04 0 0
CUI: C1854372
Disease: Impaired vibration sensation at ankles
Impaired vibration sensation at ankles 		9 0 1 1.5E-04 0 0
CUI: C1866173
Disease: BILIRUBIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1
BILIRUBIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1 		9 0 1 1.5E-04 0 0
CUI: C2931132
Disease: Crigler Najjar syndrome, type 2
Crigler Najjar syndrome, type 2 		9 0 1 1.5E-04 0 0
CUI: C2936332
Disease: Alpha-Sarcoglycanopathies
Alpha-Sarcoglycanopathies 		9 0 1 1.5E-04 0 0
CUI: C3495498
Disease: Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
Cardiomyopathy, Familial Hypertrophic, 1 (disorder) 		9 0 1 1.5E-04 0 0
CUI: C4021834
Disease: Abnormal parietal bone morphology
Abnormal parietal bone morphology 		9 0 1 1.5E-04 0 0
CUI: C4022417
Disease: Degeneration of the striatum
Degeneration of the striatum 		9 0 1 1.5E-04 0 0