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: C2675861
Disease: Lipodystrophy, Congenital Generalized, Type 3
Lipodystrophy, Congenital Generalized, Type 3 		1 0 1 6.2E-02 0 0
CUI: C2750069
Disease: Lipodystrophy, Congenital Generalized, Type 4
Lipodystrophy, Congenital Generalized, Type 4 		1 0 1 6.2E-02 0 0
CUI: C3276161
Disease: ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 2
ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 2 		1 0 1 6.2E-02 0 0
CUI: C3277426
Disease: Lack of facial subcutaneous fat
Lack of facial subcutaneous fat 		1 0 1 6.2E-02 0 0
CUI: C3502214
Disease: Microcephalic Osteodysplastic Primordial Dwarfism with Tooth Abnormalities
Microcephalic Osteodysplastic Primordial Dwarfism with Tooth Abnormalities 		1 0 1 6.2E-02 0 0
CUI: C3805917
Disease: Elevated pulmonary artery pressure
Elevated pulmonary artery pressure 		1 0 1 6.2E-02 0 0
CUI: C3807567
Disease: PARTIAL LIPODYSTROPHY, CONGENITAL CATARACTS, AND NEURODEGENERATION SYNDROME
PARTIAL LIPODYSTROPHY, CONGENITAL CATARACTS, AND NEURODEGENERATION SYNDROME 		1 0 1 6.2E-02 0 0
CUI: C3809781
Disease: Cole disease
Cole disease 		1 0 1 6.2E-02 0 0
CUI: C4016735
Disease: DIABETES MELLITUS, NONINSULIN-DEPENDENT, MODIFIER OF
DIABETES MELLITUS, NONINSULIN-DEPENDENT, MODIFIER OF 		1 0 1 6.2E-02 0 0
CUI: C4022895
Disease: Medial calcification of medium-sized arteries
Medial calcification of medium-sized arteries 		1 0 1 6.2E-02 0 0
CUI: C4022977
Disease: Increased carotid artery intimal medial thickness
Increased carotid artery intimal medial thickness 		1 0 1 6.2E-02 0 0
CUI: C4024886
Disease: Areas of hypopigmentation and hyperpigmentation that do not follow Blaschko lines
Areas of hypopigmentation and hyperpigmentation that do not follow Blaschko lines 		1 0 1 6.2E-02 0 0
CUI: C4025003
Disease: Aortic tortuosity
Aortic tortuosity 		1 0 1 6.2E-02 0 0
CUI: C4025269
Disease: Generalized arterial calcification
Generalized arterial calcification 		1 0 1 6.2E-02 0 0
CUI: C4072895
Disease: Urticarial plaque
Urticarial plaque 		1 0 1 6.2E-02 0 0
CUI: C4225406
Disease: NEUROPATHY, HEREDITARY, WITH OR WITHOUT AGE-RELATED MACULAR DEGENERATION
NEUROPATHY, HEREDITARY, WITH OR WITHOUT AGE-RELATED MACULAR DEGENERATION 		1 0 1 6.2E-02 0 0
CUI: C4285705
Disease: Pulmonary artery occlusion
Pulmonary artery occlusion 		1 0 1 6.2E-02 0 0
CUI: C4489482
Disease: Aneurysm or dissection
Aneurysm or dissection 		1 0 1 6.2E-02 0 0
CUI: C4531299
Disease: Premature occlusive vascular stenosis
Premature occlusive vascular stenosis 		1 0 1 6.2E-02 0 0
CUI: C4551985
Disease: ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 1
ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 1 		1 0 1 6.2E-02 0 0
CUI: C0020441
Disease: Hypercementosis
Hypercementosis 		2 0 1 5.9E-02 0 0
CUI: C0268351
Disease: Cutis Laxa, Autosomal Recessive, Type I
Cutis Laxa, Autosomal Recessive, Type I 		2 0 2 0.12 0 0
CUI: C0276035
Disease: Glasser's disease
Glasser's disease 		2 0 1 5.9E-02 0 0
CUI: C0343190
Disease: Cutaneous polyarteritis nodosa
Cutaneous polyarteritis nodosa 		2 0 1 5.9E-02 0 0
CUI: C0345419
Disease: Cutis marmorata telangiectatica congenita
Cutis marmorata telangiectatica congenita 		2 0 1 5.9E-02 0 0