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: C1837341
Disease: Transposition of the Great Arteries, Dextro-Looped 1
Transposition of the Great Arteries, Dextro-Looped 1 		6 0 5 0.45 0 0
CUI: C3257801
Disease: Dextrotransposition of aorta
Dextrotransposition of aorta 		4 0 4 0.40 0 0
CUI: C0344692
Disease: Isomerism of atrial appendages
Isomerism of atrial appendages 		3 0 2 0.18 0 0
CUI: C1876171
Disease: Polyasplenia
Polyasplenia 		3 0 2 0.18 0 0
CUI: C1876172
Disease: VAH, AUTOSOMAL RECESSIVE
VAH, AUTOSOMAL RECESSIVE 		3 0 2 0.18 0 0
CUI: C1876173
Disease: Heterotaxy, Visceroatrial, Autosomal Recessive
Heterotaxy, Visceroatrial, Autosomal Recessive 		3 0 2 0.18 0 0
CUI: C2910124
Disease: Isomerism of atrial appendages with asplenia or polysplenia
Isomerism of atrial appendages with asplenia or polysplenia 		3 0 2 0.18 0 0
CUI: C0040761
Disease: Transposition of Great Vessels
Transposition of Great Vessels 		61 18 10 0.16 1 5.6E-02
CUI: C0265357
Disease: Polysplenia Syndrome
Polysplenia Syndrome 		7 0 2 0.13 0 0
CUI: C0206649
Disease: Neoplasms, Fibroepithelial
Neoplasms, Fibroepithelial 		1 0 1 1.0E-01 0 0
CUI: C1708341
Disease: Heavier Menses
Heavier Menses 		1 0 1 1.0E-01 0 0
CUI: C1850644
Disease: Anterior bowing of long bones
Anterior bowing of long bones 		1 0 1 1.0E-01 0 0
CUI: C1858804
Disease: Cerebellar Ataxia, Deafness, and Narcolepsy
Cerebellar Ataxia, Deafness, and Narcolepsy 		1 0 1 1.0E-01 0 0
CUI: C1960396
Disease: Epidermal growth factor receptor negative non-small cell lung cancer
Epidermal growth factor receptor negative non-small cell lung cancer 		1 0 1 1.0E-01 0 0
CUI: C3279885
Disease: Hereditary Sensory and Autonomic Neuropathy Type Ie
Hereditary Sensory and Autonomic Neuropathy Type Ie 		1 0 1 1.0E-01 0 0
CUI: C3698541
Disease: Ohdo syndrome, Maat-Kievit-Brunner type
Ohdo syndrome, Maat-Kievit-Brunner type 		1 0 1 1.0E-01 0 0
CUI: C4021969
Disease: Abnormally straight spine
Abnormally straight spine 		1 0 1 1.0E-01 0 0
CUI: C4022856
Disease: Skewed maternal X inactivation
Skewed maternal X inactivation 		1 0 1 1.0E-01 0 0
CUI: C4025034
Disease: Abnormality of femoral epiphysis
Abnormality of femoral epiphysis 		1 0 1 1.0E-01 0 0
CUI: C4225208
Disease: MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS
MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS 		1 0 1 1.0E-01 0 0
CUI: C4274029
Disease: Biliary atresia with splenic malformation syndrome
Biliary atresia with splenic malformation syndrome 		1 0 1 1.0E-01 0 0
CUI: C4302956
Disease: Robinow-like syndrome
Robinow-like syndrome 		1 0 1 1.0E-01 0 0
CUI: C4511806
Disease: Mitotically active leiomyoma
Mitotically active leiomyoma 		1 0 1 1.0E-01 0 0
CUI: C4707795
Disease: Isolated focal cortical dysplasia
Isolated focal cortical dysplasia 		1 0 1 1.0E-01 0 0
CUI: C0175707
Disease: Asplenia Syndrome
Asplenia Syndrome 		13 0 2 9.5E-02 0 0