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: C0013124
Disease: Drinking behavior processes
Drinking behavior processes
0 31 0 0 2 1.8E-02
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele
0 9 0 0 1 1.1E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 1.2E-02
CUI: C0268140
Disease: Xeroderma pigmentosum, group F
Xeroderma pigmentosum, group F
0 31 0 0 1 8.8E-03
CUI: C0278252
Disease: Prognosis bad
Prognosis bad
0 2 0 0 1 1.2E-02
CUI: C0854076
Disease: Distal ileal obstruction syndrome
Distal ileal obstruction syndrome
0 2 0 0 2 2.4E-02
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis
0 2 0 0 1 1.2E-02
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 1.2E-02
CUI: C4511035
Disease: Isolated thrombocytopenia
Isolated thrombocytopenia
0 9 0 0 1 1.1E-02
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy
194 0 1 1.5E-03 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal
158 0 1 1.6E-03 0 0
CUI: C0231686
Disease: Gait, Unsteady
Gait, Unsteady
143 0 1 1.6E-03 0 0
CUI: C0003466
Disease: Anus, Imperforate
Anus, Imperforate
139 0 1 1.6E-03 0 0
CUI: C0393525
Disease: Progressive cerebellar ataxia
Progressive cerebellar ataxia
136 0 1 1.6E-03 0 0
Congenital ocular coloboma (disorder)
129 0 1 1.7E-03 0 0
CUI: C0234162
Disease: Cerebellar Dysmetria
Cerebellar Dysmetria
127 0 1 1.7E-03 0 0
CUI: C1860834
Disease: Infantile muscular hypotonia
Infantile muscular hypotonia
118 0 1 1.7E-03 0 0
Aplasia/Hypoplasia of the corpus callosum
108 0 1 1.7E-03 0 0
CUI: C4021759
Disease: Generalized myoclonic seizures
Generalized myoclonic seizures
105 0 1 1.7E-03 0 0
CUI: C1853487
Disease: Thick eyebrow
Thick eyebrow
104 0 1 1.7E-03 0 0
CUI: C4021085
Disease: Abnormality of brain morphology
Abnormality of brain morphology
104 0 1 1.7E-03 0 0
CUI: C4551493
Disease: Situs inversus totalis
Situs inversus totalis
104 0 1 1.7E-03 0 0
CUI: C4021786
Disease: Atypical scarring of skin
Atypical scarring of skin
101 0 1 1.7E-03 0 0
CUI: C4551488
Disease: Bifid uvula
Bifid uvula
97 0 1 1.8E-03 0 0
CUI: C0013132
Disease: Drooling
Drooling
95 0 1 1.8E-03 0 0