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: C4703620
Disease: Decreased level of GABA in serum
Decreased level of GABA in serum 		6 0 1 0.17 0 0
CUI: C0234509
Disease: Finger Agnosia
Finger Agnosia 		7 0 1 0.14 0 0
CUI: C0333227
Disease: Microembolus
Microembolus 		7 0 1 0.14 0 0
CUI: C0338630
Disease: Senile Paranoid Dementia
Senile Paranoid Dementia 		8 0 1 0.12 0 0
CUI: C0751156
Disease: FRAXA Syndrome
FRAXA Syndrome 		8 0 1 0.12 0 0
CUI: C1853934
Disease: Deposits immunoreactive to beta-amyloid protein
Deposits immunoreactive to beta-amyloid protein 		8 0 1 0.12 0 0
CUI: C0338657
Disease: Age-associated memory impairment
Age-associated memory impairment 		9 0 1 0.11 0 0
CUI: C0349081
Disease: Dementia in Parkinson's disease
Dementia in Parkinson's disease 		9 0 1 0.11 0 0
CUI: C1865903
Disease: Long-tract signs
Long-tract signs 		9 0 1 0.11 0 0
CUI: C2931784
Disease: Amyloid angiopathy
Amyloid angiopathy 		9 3 1 0.11 1 0.14
CUI: C0154038
Disease: Benign neoplasm of thyroid gland
Benign neoplasm of thyroid gland 		10 0 1 1.0E-01 0 0
CUI: C0234544
Disease: Todd Paralysis
Todd Paralysis 		10 0 1 1.0E-01 0 0
CUI: C0333101
Disease: Microaneurysm
Microaneurysm 		10 0 1 1.0E-01 0 0
CUI: C0553692
Disease: Brain hemorrhage
Brain hemorrhage 		10 0 1 1.0E-01 0 0
CUI: C1281300
Disease: Vascular degeneration
Vascular degeneration 		10 0 1 1.0E-01 0 0
CUI: C1861735
Disease: Dementia, familial Danish
Dementia, familial Danish 		10 0 1 1.0E-01 0 0
CUI: C0262376
Disease: anxiety generalized
anxiety generalized 		11 0 1 9.1E-02 0 0
CUI: C0751157
Disease: FRAXE Syndrome
FRAXE Syndrome 		11 0 1 9.1E-02 0 0
CUI: C0205858
Disease: General Paralysis
General Paralysis 		12 0 1 8.3E-02 0 0
CUI: C0233407
Disease: Disorientation
Disorientation 		12 0 1 8.3E-02 0 0
CUI: C0393911
Disease: Pure Autonomic Failure
Pure Autonomic Failure 		12 0 1 8.3E-02 0 0
CUI: C0751230
Disease: Hypothalamic Dysfunction Syndromes
Hypothalamic Dysfunction Syndromes 		12 0 1 8.3E-02 0 0
CUI: C0029810
Disease: Other specified iron deficiency anemias
Other specified iron deficiency anemias 		13 0 1 7.7E-02 0 0
CUI: C0521175
Disease: Neuropil Threads
Neuropil Threads 		13 0 1 7.7E-02 0 0
CUI: C0795875
Disease: Chromosome 21 monosomy
Chromosome 21 monosomy 		13 0 1 7.7E-02 0 0