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: C0751635
Disease: Common Carotid Artery Stenosis
Common Carotid Artery Stenosis
7 0 2 3.8E-02 0 0
CUI: C0271051
Disease: Macular retinal edema
Macular retinal edema
36 0 3 3.7E-02 0 0
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 1
8 0 2 3.7E-02 0 0
CUI: C3897877
Disease: Post-Hemorrhagic Hydrocephalus
Post-Hemorrhagic Hydrocephalus
9 0 2 3.6E-02 0 0
CUI: C1833362
Disease: Sleep-wake cycle disturbance
Sleep-wake cycle disturbance
10 0 2 3.6E-02 0 0
malignant neoplasm of head of pancreas
11 0 2 3.5E-02 0 0
Malignant neoplasm of body of pancreas
11 0 2 3.5E-02 0 0
Malignant neoplasm of tail of pancreas
11 0 2 3.5E-02 0 0
Malignant neoplasm of other specified sites of pancreas
11 0 2 3.5E-02 0 0
CUI: C0033893
Disease: Tension Headache
Tension Headache
12 0 2 3.4E-02 0 0
CUI: C0149645
Disease: Cervical myelopathy
Cervical myelopathy
12 0 2 3.4E-02 0 0
CUI: C0154822
Disease: Serous retinal detachment
Serous retinal detachment
12 0 2 3.4E-02 0 0
CUI: C4021796
Disease: Renal steatosis
Renal steatosis
12 0 2 3.4E-02 0 0
CUI: C0012619
Disease: disc disorder
disc disorder
13 0 2 3.4E-02 0 0
CUI: C0004941
Disease: Behavioral Symptoms
Behavioral Symptoms
45 0 3 3.3E-02 0 0
CUI: C0795687
Disease: Cerebral arterial thrombosis
Cerebral arterial thrombosis
14 0 2 3.3E-02 0 0
Behavioural and psychiatric symptoms of dementia
14 0 2 3.3E-02 0 0
CUI: C2362914
Disease: clinical depression
clinical depression
14 0 2 3.3E-02 0 0
CUI: C0079102
Disease: Cerebral Thrombosis
Cerebral Thrombosis
15 0 2 3.3E-02 0 0
CUI: C0221253
Disease: Xanthoma tendinosum
Xanthoma tendinosum
15 0 2 3.3E-02 0 0
CUI: C0340569
Disease: Internal Carotid Artery Stenosis
Internal Carotid Artery Stenosis
15 0 2 3.3E-02 0 0
CUI: C3714941
Disease: OTOFACIOCERVICAL SYNDROME 1
OTOFACIOCERVICAL SYNDROME 1
16 0 2 3.2E-02 0 0
CUI: C0024440
Disease: Macular Edema, Cystoid
Macular Edema, Cystoid
49 0 3 3.2E-02 0 0
CUI: C0236792
Disease: Asperger Syndrome
Asperger Syndrome
17 0 2 3.2E-02 0 0
CUI: C1392786
Disease: Cognitive changes
Cognitive changes
50 15 3 3.2E-02 1 1.1E-02