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: C3160738
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP D2
FANCONI ANEMIA, COMPLEMENTATION GROUP D2 		19 0 2 3.1E-02 0 0
CUI: C4021087
Disease: Abnormal social behavior
Abnormal social behavior 		19 0 2 3.1E-02 0 0
CUI: C0263912
Disease: Rotator cuff syndrome
Rotator cuff syndrome 		54 0 3 3.0E-02 0 0
CUI: C0338462
Disease: Semantic Dementia
Semantic Dementia 		20 0 2 3.0E-02 0 0
CUI: C0085400
Disease: Neurofibrillary degeneration (morphologic abnormality)
Neurofibrillary degeneration (morphologic abnormality) 		21 0 2 3.0E-02 0 0
CUI: C0751706
Disease: Primary Progressive Nonfluent Aphasia
Primary Progressive Nonfluent Aphasia 		21 0 2 3.0E-02 0 0
CUI: C0002940
Disease: Aneurysm
Aneurysm 		22 0 2 2.9E-02 0 0
CUI: C0577573
Disease: Mass of body region
Mass of body region 		22 0 2 2.9E-02 0 0
CUI: C1306068
Disease: After-cataract
After-cataract 		22 0 2 2.9E-02 0 0
CUI: C1275684
Disease: Meibomian gland dysfunction
Meibomian gland dysfunction 		23 0 2 2.9E-02 0 0
CUI: C0598784
Disease: Dyslipoproteinemias
Dyslipoproteinemias 		24 0 2 2.9E-02 0 0
CUI: C1527352
Disease: Hepatic Form of Wilson Disease
Hepatic Form of Wilson Disease 		24 0 2 2.9E-02 0 0
CUI: C1836926
Disease: Bone spicule pigmentation of the retina
Bone spicule pigmentation of the retina 		24 0 2 2.9E-02 0 0
CUI: C3178801
Disease: Stroke, Lacunar
Stroke, Lacunar 		24 0 2 2.9E-02 0 0
CUI: C0026961
Disease: Mydriasis
Mydriasis 		25 0 2 2.8E-02 0 0
CUI: C1842247
Disease: CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1 		25 35 2 2.8E-02 1 9.3E-03
CUI: C0015624
Disease: Fanconi Syndrome
Fanconi Syndrome 		26 0 2 2.8E-02 0 0
CUI: C0349217
Disease: Depressive episode, unspecified
Depressive episode, unspecified 		27 0 2 2.7E-02 0 0
CUI: C0523744
Disease: Lipids measurement
Lipids measurement 		27 53 2 2.7E-02 1 7.9E-03
CUI: C0751202
Disease: Cystathionine beta-Synthase Deficiency Disease
Cystathionine beta-Synthase Deficiency Disease 		27 0 2 2.7E-02 0 0
CUI: C1861537
Disease: OROFACIAL CLEFT 1
OROFACIAL CLEFT 1 		28 0 2 2.7E-02 0 0
CUI: C0022283
Disease: Incontinentia Pigmenti Achromians
Incontinentia Pigmenti Achromians 		67 0 3 2.7E-02 0 0
CUI: C0865800
Disease: asthma with copd
asthma with copd 		29 0 2 2.7E-02 0 0
CUI: C0007273
Disease: Carotid Artery Diseases
Carotid Artery Diseases 		69 6 3 2.6E-02 1 1.3E-02
CUI: C0011263
Disease: Multi-infarct dementia
Multi-infarct dementia 		30 0 2 2.6E-02 0 0