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: C0002892
Disease: Anemia, Pernicious
Anemia, Pernicious
0 4 0 0 1 4.5E-02
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele
0 9 0 0 1 3.7E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 5.3E-02
CUI: C0085292
Disease: Stiff-Person Syndrome
Stiff-Person Syndrome
0 9 0 0 1 3.7E-02
CUI: C0266295
Disease: Congenital hypoplasia of kidney
Congenital hypoplasia of kidney
0 8 0 0 2 8.0E-02
CUI: C0854076
Disease: Distal ileal obstruction syndrome
Distal ileal obstruction syndrome
0 2 0 0 2 0.11
CUI: C1321551
Disease: Shprintzen-Goldberg syndrome
Shprintzen-Goldberg syndrome
0 21 0 0 2 5.3E-02
CUI: C1840061
Disease: SMALL PATELLA SYNDROME
SMALL PATELLA SYNDROME
0 15 0 0 1 3.0E-02
CUI: C3641106
Disease: Congenital Bleeding Disorder
Congenital Bleeding Disorder
0 2 0 0 2 0.11
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 5.3E-02
CUI: C4511035
Disease: Isolated thrombocytopenia
Isolated thrombocytopenia
0 9 0 0 3 0.12
CUI: C0151889
Disease: Hyperreflexia
Hyperreflexia
539 0 1 1.5E-03 0 0
CUI: C0037369
Disease: Smoking
Smoking
391 0 1 1.9E-03 0 0
CUI: C0035229
Disease: Respiratory Insufficiency
Respiratory Insufficiency
315 0 1 2.2E-03 0 0
CUI: C0151888
Disease: Hyporeflexia
Hyporeflexia
312 0 1 2.2E-03 0 0
CUI: C1865014
Disease: Long philtrum
Long philtrum
282 0 1 2.4E-03 0 0
CUI: C0016842
Disease: Congenital pectus excavatum
Congenital pectus excavatum
272 0 1 2.4E-03 0 0
CUI: C0027066
Disease: Myoclonus
Myoclonus
265 0 1 2.5E-03 0 0
CUI: C0856975
Disease: Autistic behavior
Autistic behavior
261 0 1 2.5E-03 0 0
CUI: C1306503
Disease: Congenital exomphalos
Congenital exomphalos
235 0 1 2.6E-03 0 0
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis
595 0 2 2.7E-03 0 0
CUI: C0311394
Disease: Difficulty walking
Difficulty walking
224 0 1 2.7E-03 0 0
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
219 0 1 2.8E-03 0 0
CUI: C0029089
Disease: Ophthalmoplegia
Ophthalmoplegia
216 0 1 2.8E-03 0 0
CUI: C1843367
Disease: Poor school performance
Poor school performance
211 0 1 2.8E-03 0 0