Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Abnormality of nervous system physiology
6 0 6 0.67 0 0
CUI: C4022924
Disease: Abnormal eye physiology
Abnormal eye physiology
6 0 6 0.67 0 0
CUI: C4024924
Disease: Cerebral artery atherosclerosis
Cerebral artery atherosclerosis
6 0 6 0.67 0 0
CUI: C4025000
Disease: Myocardial steatosis
Myocardial steatosis
6 0 6 0.67 0 0
CUI: C4021654
Disease: Precocious atherosclerosis
Precocious atherosclerosis
9 0 7 0.64 0 0
Abnormal internal carotid artery morphology
7 0 6 0.60 0 0
CUI: C4021796
Disease: Renal steatosis
Renal steatosis
12 0 6 0.40 0 0
CUI: C0221253
Disease: Xanthoma tendinosum
Xanthoma tendinosum
15 0 6 0.33 0 0
CUI: C0549399
Disease: Low density lipoprotein increased
Low density lipoprotein increased
23 0 8 0.33 0 0
Familial hypercholesterolemia - homozygous
23 0 7 0.28 0 0
CUI: C0342880
Disease: Polygenic hypercholesterolemia
Polygenic hypercholesterolemia
10 0 4 0.27 0 0
CUI: C3888506
Disease: LDLR mutation
LDLR mutation
10 0 4 0.27 0 0
CUI: C0342907
Disease: Sitosterolemia
Sitosterolemia
11 0 4 0.25 0 0
CUI: C1096249
Disease: Calcification of the aorta
Calcification of the aorta
21 0 6 0.25 0 0
CUI: C0003499
Disease: Supravalvular aortic stenosis
Supravalvular aortic stenosis
23 0 6 0.23 0 0
CUI: C0151826
Disease: Retrosternal pain
Retrosternal pain
2 0 2 0.22 0 0
CUI: C0268197
Disease: Familial lipoprotein deficiency
Familial lipoprotein deficiency
2 0 2 0.22 0 0
Macrothrombocytopenia-Stomatocytosis, Mediterranean
2 0 2 0.22 0 0
CUI: C1704417
Disease: Hyperlipoproteinemia Type IIb
Hyperlipoproteinemia Type IIb
25 0 6 0.21 0 0
CUI: C0302314
Disease: Xanthoma
Xanthoma
29 0 6 0.19 0 0
CUI: C0263625
Disease: Subcutaneous calcification
Subcutaneous calcification
4 0 2 0.18 0 0
CUI: C0302164
Disease: Tuberous xanthoma
Tuberous xanthoma
4 0 2 0.18 0 0
CUI: C1859495
Disease: Episodic hemolytic anemia
Episodic hemolytic anemia
4 0 2 0.18 0 0
Low density lipoprotein receptor mutation
4 0 2 0.18 0 0
CUI: C4275075
Disease: Atypical Werner syndrome
Atypical Werner syndrome
4 0 2 0.18 0 0