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: C0018824
Disease: Heart valve disease
Heart valve disease 		0 5 0 0 1 4.3E-02
CUI: C0026703
Disease: Mucopolysaccharidoses
Mucopolysaccharidoses 		0 7 0 0 1 4.0E-02
CUI: C0026918
Disease: Mycobacterium Infections
Mycobacterium Infections 		0 14 0 0 1 3.1E-02
CUI: C0029456
Disease: Osteoporosis
Osteoporosis 		0 182 0 0 1 5.0E-03
CUI: C0036690
Disease: Septicemia
Septicemia 		0 141 0 0 1 6.3E-03
CUI: C0235031
Disease: Neurologic Symptoms
Neurologic Symptoms 		0 30 0 0 1 2.1E-02
CUI: C0243026
Disease: Sepsis
Sepsis 		0 144 0 0 1 6.2E-03
CUI: C0473527
Disease: Hypoalphalipoproteinemias
Hypoalphalipoproteinemias 		0 7 0 0 1 4.0E-02
CUI: C0600031
Disease: Congenital absence of spleen
Congenital absence of spleen 		0 6 0 0 1 4.2E-02
CUI: C0751778
Disease: Myoclonic Epilepsies, Progressive
Myoclonic Epilepsies, Progressive 		0 17 0 0 1 2.9E-02
CUI: C2350529
Disease: Pulmonary Aspergillosis
Pulmonary Aspergillosis 		0 4 0 0 1 4.5E-02
CUI: C2350530
Disease: Bronchopulmonary Aspergillosis
Bronchopulmonary Aspergillosis 		0 4 0 0 1 4.5E-02
CUI: C3258293
Disease: Valvular disease
Valvular disease 		0 1 0 0 1 5.3E-02
CUI: C4302185
Disease: Atypical Parkinsonism
Atypical Parkinsonism 		0 6 0 0 1 4.2E-02
CUI: C1856478
Disease: Hypometric horizontal saccades
Hypometric horizontal saccades 		1 0 1 1.00 0 0
CUI: C2676021
Disease: DEMENTIA, LEWY BODY, SUSCEPTIBILITY TO
DEMENTIA, LEWY BODY, SUSCEPTIBILITY TO 		1 2 1 1.00 2 0.11
CUI: C2931585
Disease: Gaucher-like disease
Gaucher-like disease 		1 0 1 1.00 0 0
CUI: C1842704
Disease: GAUCHER DISEASE, PERINATAL LETHAL
GAUCHER DISEASE, PERINATAL LETHAL 		2 18 1 0.50 9 0.32
CUI: C1856477
Disease: Slowed horizontal saccades
Slowed horizontal saccades 		3 0 1 0.33 0 0
CUI: C4024794
Disease: Horizontal supranuclear gaze palsy
Horizontal supranuclear gaze palsy 		3 0 1 0.33 0 0
CUI: C1408507
Disease: Supranuclear ophthalmoplegia
Supranuclear ophthalmoplegia 		5 0 1 0.20 0 0
CUI: C0268250
Disease: Gaucher Disease, Type 2 (disorder)
Gaucher Disease, Type 2 (disorder) 		6 34 1 0.17 19 0.56
CUI: C0348489
Disease: Other sphingolipidosis
Other sphingolipidosis 		7 0 1 0.14 0 0
CUI: C0428465
Disease: Serum lipids high (finding)
Serum lipids high (finding) 		7 0 1 0.14 0 0
CUI: C1851972
Disease: Reticular hyperpigmentation
Reticular hyperpigmentation 		7 0 1 0.14 0 0