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: C3257801
Disease: Dextrotransposition of aorta
Dextrotransposition of aorta 		4 0 4 0.67 0 0
CUI: C3536741
Disease: Discordant ventriculoarterial connection
Discordant ventriculoarterial connection 		10 0 5 0.45 0 0
CUI: C0344692
Disease: Isomerism of atrial appendages
Isomerism of atrial appendages 		3 0 2 0.29 0 0
CUI: C1876171
Disease: Polyasplenia
Polyasplenia 		3 0 2 0.29 0 0
CUI: C1876172
Disease: VAH, AUTOSOMAL RECESSIVE
VAH, AUTOSOMAL RECESSIVE 		3 0 2 0.29 0 0
CUI: C1876173
Disease: Heterotaxy, Visceroatrial, Autosomal Recessive
Heterotaxy, Visceroatrial, Autosomal Recessive 		3 0 2 0.29 0 0
CUI: C2910124
Disease: Isomerism of atrial appendages with asplenia or polysplenia
Isomerism of atrial appendages with asplenia or polysplenia 		3 0 2 0.29 0 0
CUI: C0265357
Disease: Polysplenia Syndrome
Polysplenia Syndrome 		7 0 2 0.18 0 0
CUI: C0003910
Disease: Articulation Disorders
Articulation Disorders 		1 0 1 0.17 0 0
CUI: C1850644
Disease: Anterior bowing of long bones
Anterior bowing of long bones 		1 0 1 0.17 0 0
CUI: C1971810
Disease: Congenital cardiovascular disorder
Congenital cardiovascular disorder 		1 0 1 0.17 0 0
CUI: C2675369
Disease: Chromosome 22q11.2 Microduplication Syndrome
Chromosome 22q11.2 Microduplication Syndrome 		1 0 1 0.17 0 0
CUI: C3531771
Disease: Dextrotransposition of the great arteries
Dextrotransposition of the great arteries 		1 0 1 0.17 0 0
CUI: C4016770
Disease: CONOTRUNCAL ANOMALY FACE SYNDROME/VELOCARDIOFACIAL SYNDROME
CONOTRUNCAL ANOMALY FACE SYNDROME/VELOCARDIOFACIAL SYNDROME 		1 0 1 0.17 0 0
CUI: C4021969
Disease: Abnormally straight spine
Abnormally straight spine 		1 0 1 0.17 0 0
CUI: C4025034
Disease: Abnormality of femoral epiphysis
Abnormality of femoral epiphysis 		1 0 1 0.17 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 26 1 0.17 3 8.6E-02
CUI: C4274029
Disease: Biliary atresia with splenic malformation syndrome
Biliary atresia with splenic malformation syndrome 		1 0 1 0.17 0 0
CUI: C4302956
Disease: Robinow-like syndrome
Robinow-like syndrome 		1 0 1 0.17 0 0
CUI: C0152216
Disease: Esophoria
Esophoria 		2 0 1 0.14 0 0
CUI: C0265865
Disease: Mesocardia
Mesocardia 		2 0 1 0.14 0 0
CUI: C0345065
Disease: Cervical aortic arch
Cervical aortic arch 		2 0 1 0.14 0 0
CUI: C1850640
Disease: Long eyelashes in irregular rows
Long eyelashes in irregular rows 		2 0 1 0.14 0 0
CUI: C3151189
Disease: C9 Deficiency
C9 Deficiency 		2 0 1 0.14 0 0
CUI: C4733128
Disease: familial chordoma
familial chordoma 		2 0 1 0.14 0 0