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: C1838577
Disease: Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy 		7 0 5 0.12 0 0
CUI: C0878486
Disease: Arteriolosclerosis
Arteriolosclerosis 		13 0 5 0.10 0 0
CUI: C0085280
Disease: Alagille Syndrome
Alagille Syndrome 		38 0 7 9.9E-02 0 0
CUI: C2733158
Disease: Cerebral Small Vessel Diseases
Cerebral Small Vessel Diseases 		62 0 9 9.7E-02 0 0
CUI: C0268393
Disease: Familial Cerebral Amyloid Angiopathy
Familial Cerebral Amyloid Angiopathy 		18 0 5 9.4E-02 0 0
CUI: C1510489
Disease: Cerebral Amyloid Angiopathy, Hereditary
Cerebral Amyloid Angiopathy, Hereditary 		19 0 5 9.3E-02 0 0
CUI: C0265268
Disease: Adams Oliver syndrome
Adams Oliver syndrome 		9 0 4 8.9E-02 0 0
CUI: C3888088
Disease: SMITH-MCCORT DYSPLASIA 1
SMITH-MCCORT DYSPLASIA 1 		62 0 8 8.5E-02 0 0
CUI: C1263858
Disease: Muscular dystrophy congenital, merosin negative
Muscular dystrophy congenital, merosin negative 		12 0 4 8.3E-02 0 0
CUI: C1860405
Disease: Snowflake vitreoretinal degeneration
Snowflake vitreoretinal degeneration 		15 0 4 7.8E-02 0 0
CUI: C1260873
Disease: Aortic valve disorder
Aortic valve disorder 		58 0 7 7.7E-02 0 0
CUI: C4707243
Disease: Familial thoracic aortic aneurysm and aortic dissection
Familial thoracic aortic aneurysm and aortic dissection 		59 0 7 7.6E-02 0 0
CUI: C4551482
Disease: Adams-Oliver syndrome 1
Adams-Oliver syndrome 1 		17 0 4 7.5E-02 0 0
CUI: C0012736
Disease: Dissecting aortic aneurysm
Dissecting aortic aneurysm 		18 0 4 7.4E-02 0 0
CUI: C0266568
Disease: Persistent Hyperplastic Primary Vitreous
Persistent Hyperplastic Primary Vitreous 		33 0 5 7.4E-02 0 0
CUI: C0268407
Disease: Senile cardiac amyloidosis
Senile cardiac amyloidosis 		33 0 5 7.4E-02 0 0
CUI: C0520574
Disease: Cerebrovascular amyloidosis
Cerebrovascular amyloidosis 		4 0 3 7.3E-02 0 0
CUI: C0151860
Disease: Acquired porencephaly
Acquired porencephaly 		34 0 5 7.2E-02 0 0
CUI: C0206368
Disease: Exfoliation Syndrome
Exfoliation Syndrome 		94 0 9 7.2E-02 0 0
CUI: C0085220
Disease: Cerebral Amyloid Angiopathy
Cerebral Amyloid Angiopathy 		65 0 7 7.1E-02 0 0
CUI: C0268392
Disease: Localized amyloidosis
Localized amyloidosis 		5 0 3 7.1E-02 0 0
CUI: C1527383
Disease: Morphea
Morphea 		20 0 4 7.1E-02 0 0
CUI: C2931672
Disease: Cerebral hemorrhage with amyloidosis, hereditary, Dutch type
Cerebral hemorrhage with amyloidosis, hereditary, Dutch type 		20 0 4 7.1E-02 0 0
CUI: C0079474
Disease: Hallopeau-Siemens Disease
Hallopeau-Siemens Disease 		51 0 6 7.1E-02 0 0
CUI: C0342199
Disease: Iodine deficiency syndrome
Iodine deficiency syndrome 		22 0 4 6.9E-02 0 0