Source: INFERRED ×
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: C1851959
Disease: Fluctuations in consciousness
Fluctuations in consciousness 		10 0 3 0.20 0 0
CUI: C1969363
Disease: Middle age onset
Middle age onset 		5 0 2 0.18 0 0
CUI: C4531121
Disease: Monotonic speech
Monotonic speech 		9 0 2 0.13 0 0
CUI: C0233763
Disease: Hallucinations, Visual
Hallucinations, Visual 		18 0 3 0.13 0 0
CUI: C0020479
Disease: Hyperlipoproteinemia Type III
Hyperlipoproteinemia Type III 		1 0 1 0.12 0 0
CUI: C0268250
Disease: Gaucher Disease, Type 2 (disorder)
Gaucher Disease, Type 2 (disorder) 		1 25 1 0.12 7 0.21
CUI: C0268251
Disease: Gaucher Disease, Type 3 (disorder)
Gaucher Disease, Type 3 (disorder) 		1 24 1 0.12 7 0.21
CUI: C0523511
Disease: Apolipoproteins E measurement (procedure)
Apolipoproteins E measurement (procedure) 		1 1 1 0.12 1 6.2E-02
CUI: C1836904
Disease: Spastic/hyperactive bladder
Spastic/hyperactive bladder 		10 0 2 0.12 0 0
CUI: C1842704
Disease: GAUCHER DISEASE, PERINATAL LETHAL
GAUCHER DISEASE, PERINATAL LETHAL 		1 16 1 0.12 7 0.28
CUI: C1856476
Disease: Gaucher Disease, Type Iiic
Gaucher Disease, Type Iiic 		1 19 1 0.12 7 0.25
CUI: C1856478
Disease: Hypometric horizontal saccades
Hypometric horizontal saccades 		1 0 1 0.12 0 0
CUI: C1863051
Disease: ALZHEIMER DISEASE 2
ALZHEIMER DISEASE 2 		1 1 1 0.12 1 6.2E-02
CUI: C1868595
Disease: PARKINSON DISEASE 1, AUTOSOMAL DOMINANT (disorder)
PARKINSON DISEASE 1, AUTOSOMAL DOMINANT (disorder) 		1 3 1 0.12 1 5.6E-02
CUI: C2673196
Disease: LIPOPROTEIN GLOMERULOPATHY
LIPOPROTEIN GLOMERULOPATHY 		1 0 1 0.12 0 0
CUI: C2676021
Disease: DEMENTIA, LEWY BODY, SUSCEPTIBILITY TO
DEMENTIA, LEWY BODY, SUSCEPTIBILITY TO 		1 2 1 0.12 1 5.9E-02
CUI: C4015869
Disease: APOE2-DUNEDIN PHENOTYPE
APOE2-DUNEDIN PHENOTYPE 		1 0 1 0.12 0 0
CUI: C4015877
Disease: APOE3(-)-FREIBURG PHENOTYPE
APOE3(-)-FREIBURG PHENOTYPE 		1 0 1 0.12 0 0
CUI: C4015878
Disease: APOE4 VARIANT PHENOTYPE
APOE4 VARIANT PHENOTYPE 		1 0 1 0.12 0 0
CUI: C4015880
Disease: APOE2 VARIANT PHENOTYPE
APOE2 VARIANT PHENOTYPE 		1 0 1 0.12 0 0
CUI: C4015881
Disease: APOE4(+) PHENOTYPE
APOE4(+) PHENOTYPE 		1 0 1 0.12 0 0
CUI: C4025650
Disease: Abnormality of lipid metabolism
Abnormality of lipid metabolism 		1 0 1 0.12 0 0
CUI: C4479658
Disease: HYPERLIPOPROTEINEMIA, TYPE III, AND ATHEROSCLEROSIS ASSOCIATED WITH APOE5
HYPERLIPOPROTEINEMIA, TYPE III, AND ATHEROSCLEROSIS ASSOCIATED WITH APOE5 		1 0 1 0.12 0 0
CUI: C4479660
Disease: APOE5 VARIANT
APOE5 VARIANT 		1 0 1 0.12 0 0
CUI: C4540478
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 52
MENTAL RETARDATION, AUTOSOMAL DOMINANT 52 		1 0 1 0.12 0 0