Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Acute idiopathic thrombocytopenic purpura
0 1 0 0 1 1.0E-02
CUI: C0863104
Disease: Neck discomfort
Neck discomfort
0 2 0 0 1 1.0E-02
CUI: C0008810
Disease: Circadian Rhythms
Circadian Rhythms
45 0 1 3.9E-04 0 0
Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus
43 0 1 3.9E-04 0 0
CUI: C1855672
Disease: Immotile cilia
Immotile cilia
41 0 1 3.9E-04 0 0
Attenuation of retinal blood vessels
41 0 1 3.9E-04 0 0
Impaired nasal mucociliary clearance
41 0 1 3.9E-04 0 0
LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY
40 0 1 3.9E-04 0 0
CUI: C1839603
Disease: Proximal tubulopathy
Proximal tubulopathy
37 0 1 3.9E-04 0 0
Leigh Syndrome due to Mitochondrial Complex IV Deficiency
37 0 1 3.9E-04 0 0
Leigh Syndrome Due To Mitochondrial Complex II Deficiency
36 0 1 3.9E-04 0 0
Leigh Syndrome due to Mitochondrial Complex III Deficiency
36 0 1 3.9E-04 0 0
Leigh Syndrome due to Mitochondrial Complex V Deficiency
36 0 1 3.9E-04 0 0
Necrotizing encephalopathy, infantile subacute, of Leigh
36 0 1 3.9E-04 0 0
CUI: C4025844
Disease: Abnormal chorioretinal morphology
Abnormal chorioretinal morphology
36 0 1 3.9E-04 0 0
CUI: C1865060
Disease: Molar tooth sign on MRI
Molar tooth sign on MRI
35 0 1 3.9E-04 0 0
CUI: C4317124
Disease: Polynesian Bronchiectasis
Polynesian Bronchiectasis
35 0 1 3.9E-04 0 0
CUI: C1295585
Disease: Decreased vibratory sense
Decreased vibratory sense
33 0 1 3.9E-04 0 0
Night blindness, congenital stationary
32 0 1 3.9E-04 0 0
CUI: C1844020
Disease: HETEROTAXY, VISCERAL, 1, X-LINKED
HETEROTAXY, VISCERAL, 1, X-LINKED
30 0 1 3.9E-04 0 0
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED
30 0 1 3.9E-04 0 0
CUI: C3553676
Disease: HETEROTAXY, VISCERAL, 6, AUTOSOMAL
HETEROTAXY, VISCERAL, 6, AUTOSOMAL
30 0 1 3.9E-04 0 0
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal
29 0 1 3.9E-04 0 0
CUI: C3151057
Disease: HETEROTAXY, VISCERAL, 4, AUTOSOMAL
HETEROTAXY, VISCERAL, 4, AUTOSOMAL
29 0 1 3.9E-04 0 0
CUI: C3808249
Disease: Abnormality of the optic disc
Abnormality of the optic disc
26 0 1 3.9E-04 0 0