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: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 5.4E-03
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis
0 1 0 0 1 5.4E-03
Acute idiopathic thrombocytopenic purpura
0 1 0 0 1 5.4E-03
CUI: C0863104
Disease: Neck discomfort
Neck discomfort
0 2 0 0 2 1.1E-02
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 5.4E-03
Abnormal mitochondria in muscle tissue
39 0 1 3.1E-04 0 0
CUI: C1295585
Disease: Decreased vibratory sense
Decreased vibratory sense
33 0 1 3.1E-04 0 0
CUI: C1844020
Disease: HETEROTAXY, VISCERAL, 1, X-LINKED
HETEROTAXY, VISCERAL, 1, X-LINKED
30 0 1 3.1E-04 0 0
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED
30 0 1 3.1E-04 0 0
CUI: C3553676
Disease: HETEROTAXY, VISCERAL, 6, AUTOSOMAL
HETEROTAXY, VISCERAL, 6, AUTOSOMAL
30 0 1 3.1E-04 0 0
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal
29 0 1 3.1E-04 0 0
CUI: C3151057
Disease: HETEROTAXY, VISCERAL, 4, AUTOSOMAL
HETEROTAXY, VISCERAL, 4, AUTOSOMAL
29 0 1 3.1E-04 0 0
CUI: C0155707
Disease: Trifascicular block
Trifascicular block
23 0 1 3.1E-04 0 0
CUI: C0520886
Disease: ST segment elevation (finding)
ST segment elevation (finding)
23 0 1 3.1E-04 0 0
CUI: C1846347
Disease: Renal salt wasting
Renal salt wasting
22 0 1 3.1E-04 0 0
CUI: C0272002
Disease: alpha^0^ Thalassemia
alpha^0^ Thalassemia
21 0 1 3.1E-04 0 0
CUI: C3894553
Disease: response to simvastatin
response to simvastatin
21 0 1 3.1E-04 0 0
CUI: C1845123
Disease: Generalized neonatal hypotonia
Generalized neonatal hypotonia
20 0 1 3.1E-04 0 0
CUI: C2936862
Disease: Bardet-Biedl syndrome 1 (disorder)
Bardet-Biedl syndrome 1 (disorder)
20 0 1 3.1E-04 0 0
Juvenile amyotrophic lateral sclerosis
20 0 1 3.1E-04 0 0
CUI: C4022735
Disease: Cerebral white matter atrophy
Cerebral white matter atrophy
20 0 1 3.1E-04 0 0
CUI: C0334013
Disease: Phrynoderma
Phrynoderma
19 0 1 3.1E-04 0 0
Congenital disorder of glycosylation type 1s
19 0 1 3.1E-04 0 0
Dehydroepiandrosterone sulfate measurement (procedure)
18 0 1 3.1E-04 0 0
CUI: C0271185
Disease: Metamorphopsia
Metamorphopsia
18 0 1 3.1E-04 0 0