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: C0151467
Disease: Addisonian crisis
Addisonian crisis 		4 0 1 0.14 0 0
CUI: C0520574
Disease: Cerebrovascular amyloidosis
Cerebrovascular amyloidosis 		4 0 1 0.14 0 0
CUI: C0749263
Disease: temporal pain
temporal pain 		4 0 1 0.14 0 0
CUI: C1863052
Disease: ALZHEIMER DISEASE, FAMILIAL, 1
ALZHEIMER DISEASE, FAMILIAL, 1 		4 0 1 0.14 0 0
CUI: C0268392
Disease: Localized amyloidosis
Localized amyloidosis 		5 0 1 0.12 0 0
CUI: C0268595
Disease: Glutaric aciduria, type 1
Glutaric aciduria, type 1 		5 0 1 0.12 0 0
CUI: C0338582
Disease: Sporadic Cerebral Amyloid Angiopathy
Sporadic Cerebral Amyloid Angiopathy 		6 0 1 0.11 0 0
CUI: C1332655
Disease: Complement component 3 deficiency
Complement component 3 deficiency 		6 0 1 0.11 0 0
CUI: C4703620
Disease: Decreased level of GABA in serum
Decreased level of GABA in serum 		6 0 1 0.11 0 0
CUI: C1849156
Disease: Spastic Ataxia
Spastic Ataxia 		28 0 3 0.10 0 0
CUI: C0003079
Disease: Anisocoria
Anisocoria 		7 0 1 1.0E-01 0 0
CUI: C0234509
Disease: Finger Agnosia
Finger Agnosia 		7 0 1 1.0E-01 0 0
CUI: C0333227
Disease: Microembolus
Microembolus 		7 0 1 1.0E-01 0 0
CUI: C0338630
Disease: Senile Paranoid Dementia
Senile Paranoid Dementia 		8 0 1 9.1E-02 0 0
CUI: C0751156
Disease: FRAXA Syndrome
FRAXA Syndrome 		8 0 1 9.1E-02 0 0
CUI: C1853934
Disease: Deposits immunoreactive to beta-amyloid protein
Deposits immunoreactive to beta-amyloid protein 		8 0 1 9.1E-02 0 0
CUI: C1833662
Disease: INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE AND FRONTOTEMPORAL DEMENTIA
INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE AND FRONTOTEMPORAL DEMENTIA 		34 0 3 8.6E-02 0 0
CUI: C0338657
Disease: Age-associated memory impairment
Age-associated memory impairment 		9 0 1 8.3E-02 0 0
CUI: C0349081
Disease: Dementia in Parkinson's disease
Dementia in Parkinson's disease 		9 0 1 8.3E-02 0 0
CUI: C1865903
Disease: Long-tract signs
Long-tract signs 		9 0 1 8.3E-02 0 0
CUI: C2931784
Disease: Amyloid angiopathy
Amyloid angiopathy 		9 0 1 8.3E-02 0 0
CUI: C4021779
Disease: Abnormality of the calf musculature
Abnormality of the calf musculature 		9 0 1 8.3E-02 0 0
CUI: C4054695
Disease: Familial glucocorticoid deficiency
Familial glucocorticoid deficiency 		9 0 1 8.3E-02 0 0
CUI: C0154038
Disease: Benign neoplasm of thyroid gland
Benign neoplasm of thyroid gland 		10 0 1 7.7E-02 0 0
CUI: C0234544
Disease: Todd Paralysis
Todd Paralysis 		10 0 1 7.7E-02 0 0