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: C2678038
Disease: Alopecia, Androgenetic, 2
Alopecia, Androgenetic, 2 		39 0 1 9.0E-04 0 0
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome 		39 0 1 9.0E-04 0 0
CUI: C4049090
Disease: Alopecia, Androgenetic, 1
Alopecia, Androgenetic, 1 		39 0 1 9.0E-04 0 0
CUI: C1838681
Disease: Rapidly progressive
Rapidly progressive 		38 0 1 9.0E-04 0 0
CUI: C4025844
Disease: Abnormal chorioretinal morphology
Abnormal chorioretinal morphology 		36 0 1 9.0E-04 0 0
CUI: C1720164
Disease: Central corneal thickness
Central corneal thickness 		35 0 1 9.0E-04 0 0
CUI: C4317124
Disease: Polynesian Bronchiectasis
Polynesian Bronchiectasis 		35 0 1 9.0E-04 0 0
CUI: C1292772
Disease: Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative
Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative 		32 0 1 9.1E-04 0 0
CUI: C1837066
Disease: Recurrent viral infection
Recurrent viral infection 		32 0 1 9.1E-04 0 0
CUI: C1850135
Disease: Flared metaphysis
Flared metaphysis 		32 0 1 9.1E-04 0 0
CUI: C1850573
Disease: Slender build
Slender build 		31 0 1 9.1E-04 0 0
CUI: C0006157
Disease: Breech Presentation
Breech Presentation 		30 0 1 9.1E-04 0 0
CUI: C1844020
Disease: HETEROTAXY, VISCERAL, 1, X-LINKED
HETEROTAXY, VISCERAL, 1, X-LINKED 		30 0 1 9.1E-04 0 0
CUI: C3151867
Disease: CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED 		30 0 1 9.1E-04 0 0
CUI: C3553676
Disease: HETEROTAXY, VISCERAL, 6, AUTOSOMAL
HETEROTAXY, VISCERAL, 6, AUTOSOMAL 		30 0 1 9.1E-04 0 0
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal 		29 0 1 9.1E-04 0 0
CUI: C2677328
Disease: Cerebral hypomyelination
Cerebral hypomyelination 		29 0 1 9.1E-04 0 0
CUI: C3151057
Disease: HETEROTAXY, VISCERAL, 4, AUTOSOMAL
HETEROTAXY, VISCERAL, 4, AUTOSOMAL 		29 0 1 9.1E-04 0 0
CUI: C3853779
Disease: Neonatal Alloimmune Thrombocytopenia
Neonatal Alloimmune Thrombocytopenia 		29 0 1 9.1E-04 0 0
CUI: C4024737
Disease: Aplasia/Hypoplasia of the skin
Aplasia/Hypoplasia of the skin 		29 0 1 9.1E-04 0 0
CUI: C4024996
Disease: Aplasia/Hypoplasia of the lungs
Aplasia/Hypoplasia of the lungs 		29 0 1 9.1E-04 0 0
CUI: C1843697
Disease: Axial muscle weakness
Axial muscle weakness 		28 0 1 9.1E-04 0 0
CUI: C0020630
Disease: Hypophosphatasia
Hypophosphatasia 		27 0 1 9.1E-04 0 0
CUI: C0497406
Disease: Overweight
Overweight 		27 0 1 9.1E-04 0 0
CUI: C1446712
Disease: Overlapping fingers
Overlapping fingers 		27 0 1 9.1E-04 0 0