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: C1330966
Disease: Developmental Academic Disorder
Developmental Academic Disorder 		29 0 3 3.8E-02 0 0
CUI: C1859828
Disease: Increased extraneuronal autofluorescent lipopigment
Increased extraneuronal autofluorescent lipopigment 		2 0 2 3.8E-02 0 0
CUI: C2677294
Disease: Atrial Fibrillation, Familial, 6
Atrial Fibrillation, Familial, 6 		2 0 2 3.8E-02 0 0
CUI: C3810401
Disease: ATRIAL STANDSTILL 2
ATRIAL STANDSTILL 2 		2 0 2 3.8E-02 0 0
CUI: C0151785
Disease: Disease of mucous membrane
Disease of mucous membrane 		30 0 3 3.8E-02 0 0
CUI: C1442837
Disease: Myocardial necrosis
Myocardial necrosis 		30 0 3 3.8E-02 0 0
CUI: C0038826
Disease: Superinfection
Superinfection 		85 0 5 3.8E-02 0 0
CUI: C0014040
Disease: Encephalitis Lethargica
Encephalitis Lethargica 		3 0 2 3.8E-02 0 0
CUI: C0234972
Disease: Convulsive disorder
Convulsive disorder 		3 0 2 3.8E-02 0 0
CUI: C0333641
Disease: Atrophic
Atrophic 		58 0 4 3.8E-02 0 0
CUI: C1850447
Disease: Rectilinear intracellular accumulation of autofluorescent lipopigment storage material
Rectilinear intracellular accumulation of autofluorescent lipopigment storage material 		3 0 2 3.8E-02 0 0
CUI: C1850451
Disease: CEROID LIPOFUSCINOSIS, NEURONAL, 1
CEROID LIPOFUSCINOSIS, NEURONAL, 1 		3 0 2 3.8E-02 0 0
CUI: C1853623
Disease: Fryns-Aftimos Syndrome
Fryns-Aftimos Syndrome 		3 0 2 3.8E-02 0 0
CUI: C1395512
Disease: Placental dysfunction
Placental dysfunction 		31 0 3 3.7E-02 0 0
CUI: C0242184
Disease: Hypoxia
Hypoxia 		59 0 4 3.7E-02 0 0
CUI: C1959635
Disease: Parvovirus B19 (disease)
Parvovirus B19 (disease) 		59 0 4 3.7E-02 0 0
CUI: C0007286
Disease: Carpal Tunnel Syndrome
Carpal Tunnel Syndrome 		87 0 5 3.7E-02 0 0
CUI: C0238190
Disease: Inclusion Body Myositis (disorder)
Inclusion Body Myositis (disorder) 		87 0 5 3.7E-02 0 0
CUI: C4076349
Disease: Chronic alcoholic liver disease
Chronic alcoholic liver disease 		4 0 2 3.7E-02 0 0
CUI: C4316899
Disease: Cystinosis
Cystinosis 		32 0 3 3.7E-02 0 0
CUI: C0002622
Disease: Amnesia
Amnesia 		173 0 8 3.7E-02 0 0
CUI: C1708350
Disease: Hereditary Leiomyomatosis and Renal Cell Cancer
Hereditary Leiomyomatosis and Renal Cell Cancer 		61 0 4 3.7E-02 0 0
CUI: C1533217
Disease: Methamphetamine dependence
Methamphetamine dependence 		33 0 3 3.7E-02 0 0
CUI: C0410422
Disease: Chronic multifocal osteomyelitis
Chronic multifocal osteomyelitis 		34 0 3 3.6E-02 0 0
CUI: C3665346
Disease: Unspecified visual loss
Unspecified visual loss 		235 0 10 3.6E-02 0 0