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: C4551493
Disease: Situs inversus totalis
Situs inversus totalis
104 0 1 4.5E-03 0 0
CUI: C0266449
Disease: Congenital anomaly of brain
Congenital anomaly of brain
103 0 1 4.6E-03 0 0
CUI: C0003706
Disease: Arachnodactyly
Arachnodactyly
102 0 1 4.6E-03 0 0
CUI: C0017639
Disease: Gliosis
Gliosis
102 0 1 4.6E-03 0 0
Congenital Disorders of Glycosylation
102 0 1 4.6E-03 0 0
CUI: C0857490
Disease: Granulocyte count
Granulocyte count
100 0 1 4.6E-03 0 0
CUI: C1840379
Disease: Cerebellar vermis hypoplasia
Cerebellar vermis hypoplasia
100 0 1 4.6E-03 0 0
CUI: C0151888
Disease: Hyporeflexia
Hyporeflexia
312 0 2 4.7E-03 0 0
CUI: C4025814
Disease: Abnormality of the metaphysis
Abnormality of the metaphysis
97 0 1 4.7E-03 0 0
CUI: C0240379
Disease: Open mouth (finding)
Open mouth (finding)
96 0 1 4.7E-03 0 0
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement
96 0 1 4.7E-03 0 0
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis
95 0 1 4.7E-03 0 0
CUI: C0020598
Disease: Hypocalcemia
Hypocalcemia
94 0 1 4.8E-03 0 0
CUI: C0026266
Disease: Mitral Valve Insufficiency
Mitral Valve Insufficiency
94 0 1 4.8E-03 0 0
CUI: C0085583
Disease: Choreoathetosis
Choreoathetosis
94 0 1 4.8E-03 0 0
CUI: C0850703
Disease: Frequent falls
Frequent falls
94 0 1 4.8E-03 0 0
CUI: C0020626
Disease: Hypoparathyroidism
Hypoparathyroidism
92 0 1 4.8E-03 0 0
CUI: C1456873
Disease: alpha^+^ Thalassemia
alpha^+^ Thalassemia
92 0 1 4.8E-03 0 0
CUI: C0029434
Disease: Osteogenesis Imperfecta
Osteogenesis Imperfecta
90 0 1 4.9E-03 0 0
CUI: C0003119
Disease: Anophthalmos
Anophthalmos
89 0 1 4.9E-03 0 0
CUI: C0014553
Disease: Absence Epilepsy
Absence Epilepsy
89 0 1 4.9E-03 0 0
CUI: C0086237
Disease: Epilepsy, Cryptogenic
Epilepsy, Cryptogenic
88 0 1 4.9E-03 0 0
CUI: C0271270
Disease: Oculovestibuloauditory syndrome
Oculovestibuloauditory syndrome
87 0 1 4.9E-03 0 0
CUI: C1837463
Disease: Narrow face
Narrow face
87 0 1 4.9E-03 0 0
CUI: C0002312
Disease: alpha-Thalassemia
alpha-Thalassemia
86 0 1 5.0E-03 0 0