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: C0003578
Disease: Apnea
Apnea
262 0 1 3.8E-03 0 0
CUI: C0004134
Disease: Ataxia
Ataxia
868 0 1 1.2E-03 0 0
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
1758 0 1 5.7E-04 0 0
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
502 0 1 2.0E-03 0 0
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis
595 0 1 1.7E-03 0 0
CUI: C0009806
Disease: Constipation
Constipation
424 0 1 2.4E-03 0 0
CUI: C0011570
Disease: Mental Depression
Mental Depression
1478 0 1 6.8E-04 0 0
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
1719 0 1 5.8E-04 0 0
CUI: C0011603
Disease: Dermatitis
Dermatitis
496 0 1 2.0E-03 0 0
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy
645 0 1 1.6E-03 0 0
CUI: C0014065
Disease: Congenital cerebral hernia
Congenital cerebral hernia
93 0 1 1.1E-02 0 0
CUI: C0014474
Disease: Ependymoma
Ependymoma
244 0 1 4.1E-03 0 0
CUI: C0015732
Disease: Fecal Incontinence
Fecal Incontinence
60 0 1 1.7E-02 0 0
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II
194 0 1 5.2E-03 0 0
CUI: C0019569
Disease: Hirschsprung Disease
Hirschsprung Disease
384 0 1 2.6E-03 0 0
CUI: C0020255
Disease: Hydrocephalus
Hydrocephalus
473 0 1 2.1E-03 0 0
CUI: C0024530
Disease: Malaria
Malaria
685 0 1 1.5E-03 0 0
CUI: C0025202
Disease: melanoma
melanoma
3087 0 1 3.2E-04 0 0
CUI: C0025362
Disease: Mental Retardation
Mental Retardation
505 0 1 2.0E-03 0 0
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia
967 0 1 1.0E-03 0 0
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
6385 0 1 1.6E-04 0 0
CUI: C0027651
Disease: Neoplasms
Neoplasms
10161 0 1 9.8E-05 0 0
CUI: C0028738
Disease: Nystagmus
Nystagmus
833 0 1 1.2E-03 0 0
CUI: C0029453
Disease: Osteopenia
Osteopenia
845 0 1 1.2E-03 0 0
CUI: C0033377
Disease: Ptosis
Ptosis
607 0 1 1.6E-03 0 0