Source: ALL
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: C1857970
Disease: Hypobetalipoproteinemia, Familial, 2
Hypobetalipoproteinemia, Familial, 2 		3 0 2 0.67 0 0
CUI: C0523509
Disease: Apolipoprotein B Assay
Apolipoprotein B Assay 		1 0 1 0.50 0 0
CUI: C1704299
Disease: Hypobetalipoproteinemia, Familial, Apolipoprotein B
Hypobetalipoproteinemia, Familial, Apolipoprotein B 		1 0 1 0.50 0 0
CUI: C3888316
Disease: Hypercholesterolemia, familial, due to ligand-defective apolipoprotein B
Hypercholesterolemia, familial, due to ligand-defective apolipoprotein B 		1 0 1 0.50 0 0
CUI: C0239549
Disease: Fat intolerance
Fat intolerance 		2 0 1 0.33 0 0
CUI: C0268197
Disease: Familial lipoprotein deficiency
Familial lipoprotein deficiency 		2 0 1 0.33 0 0
CUI: C1272174
Disease: Scotopic sensitivity
Scotopic sensitivity 		2 0 1 0.33 0 0
CUI: C0259771
Disease: Steatocystoma multiplex
Steatocystoma multiplex 		3 0 1 0.25 0 0
CUI: C0853085
Disease: Decreased LDL cholesterol concentration
Decreased LDL cholesterol concentration 		9 0 2 0.22 0 0
CUI: C2919414
Disease: Low density lipoprotein receptor mutation
Low density lipoprotein receptor mutation 		4 0 1 0.20 0 0
CUI: C0035528
Disease: Riboflavin Deficiency
Riboflavin Deficiency 		5 0 1 0.17 0 0
CUI: C1862596
Disease: Familial hypobetalipoproteinemia
Familial hypobetalipoproteinemia 		12 24 2 0.17 2 5.1E-02
CUI: C3151466
Disease: HEPATIC LIPASE DEFICIENCY (disorder)
HEPATIC LIPASE DEFICIENCY (disorder) 		5 0 1 0.17 0 0
CUI: C0268601
Disease: HMG CoA lyase deficiency
HMG CoA lyase deficiency 		6 0 1 0.14 0 0
CUI: C1262005
Disease: Ischaemic cerebral infarction
Ischaemic cerebral infarction 		6 0 1 0.14 0 0
CUI: C1720505
Disease: Adult growth hormone deficiency
Adult growth hormone deficiency 		6 0 1 0.14 0 0
CUI: C2239120
Disease: eyelids (symptom)
eyelids (symptom) 		6 0 1 0.14 0 0
CUI: C4022811
Disease: Abnormality of nervous system physiology
Abnormality of nervous system physiology 		6 0 1 0.14 0 0
CUI: C4022924
Disease: Abnormal eye physiology
Abnormal eye physiology 		6 0 1 0.14 0 0
CUI: C4024924
Disease: Cerebral artery atherosclerosis
Cerebral artery atherosclerosis 		6 0 1 0.14 0 0
CUI: C4025000
Disease: Myocardial steatosis
Myocardial steatosis 		6 0 1 0.14 0 0
CUI: C1860488
Disease: Abnormal internal carotid artery morphology
Abnormal internal carotid artery morphology 		7 0 1 0.12 0 0
CUI: C0242084
Disease: Ruptured cerebral aneurysm
Ruptured cerebral aneurysm 		8 0 1 0.11 0 0
CUI: C0687751
Disease: Acanthocytosis
Acanthocytosis 		8 0 1 0.11 0 0
CUI: C4087498
Disease: Familial LCAT deficiency
Familial LCAT deficiency 		8 0 1 0.11 0 0