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: C0015338
Disease: Exstrophy
Exstrophy 		1 0 1 6.7E-02 0 0
CUI: C0158667
Disease: Aplasia of Lacrimal and Salivary Glands
Aplasia of Lacrimal and Salivary Glands 		1 0 1 6.7E-02 0 0
CUI: C0265914
Disease: Anomalous pulmonary vein
Anomalous pulmonary vein 		1 0 1 6.7E-02 0 0
CUI: C0266336
Disease: Congenital absence of bladder
Congenital absence of bladder 		1 0 1 6.7E-02 0 0
CUI: C0267581
Disease: Rectal Stenosis
Rectal Stenosis 		1 0 1 6.7E-02 0 0
CUI: C0341154
Disease: Esophageal atresia with tracheoesophageal fistula (disorder)
Esophageal atresia with tracheoesophageal fistula (disorder) 		1 0 1 6.7E-02 0 0
CUI: C0344787
Disease: Complete atrioventricular septal defect
Complete atrioventricular septal defect 		1 0 1 6.7E-02 0 0
CUI: C0344923
Disease: Multiple ventricular septal defects
Multiple ventricular septal defects 		1 0 1 6.7E-02 0 0
CUI: C0795812
Disease: Chromosome 4, trisomy 4q
Chromosome 4, trisomy 4q 		1 0 1 6.7E-02 0 0
CUI: C0795868
Disease: Chromosome 18, tetrasomy 18p
Chromosome 18, tetrasomy 18p 		1 0 1 6.7E-02 0 0
CUI: C0795939
Disease: AMINOPTERIN SYNDROME SINE AMINOPTERIN
AMINOPTERIN SYNDROME SINE AMINOPTERIN 		1 0 1 6.7E-02 0 0
CUI: C1845108
Disease: Prominent median palatal raphe
Prominent median palatal raphe 		1 0 1 6.7E-02 0 0
CUI: C1845292
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP B
FANCONI ANEMIA, COMPLEMENTATION GROUP B 		1 0 1 6.7E-02 0 0
CUI: C1848600
Disease: Vater Association With Hydrocephalus
Vater Association With Hydrocephalus 		1 0 1 6.7E-02 0 0
CUI: C1861348
Disease: Syndactyly, type v
Syndactyly, type v 		1 0 1 6.7E-02 0 0
CUI: C1861350
Disease: Enlarged proximal interphalangeal joints
Enlarged proximal interphalangeal joints 		1 0 1 6.7E-02 0 0
CUI: C1862139
Disease: Brachymesophalangy 2 and 5
Brachymesophalangy 2 and 5 		1 0 1 6.7E-02 0 0
CUI: C1968843
Disease: MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 5 (disorder)
MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 5 (disorder) 		1 0 1 6.7E-02 0 0
CUI: C2675862
Disease: Pyloric Stenosis, Infantile Hypertrophic, 5
Pyloric Stenosis, Infantile Hypertrophic, 5 		1 0 1 6.7E-02 0 0
CUI: C3839990
Disease: Congenital stenosis of nasal pyriform aperture
Congenital stenosis of nasal pyriform aperture 		1 0 1 6.7E-02 0 0
CUI: C4016468
Disease: VACTERL ASSOCIATION, X-LINKED
VACTERL ASSOCIATION, X-LINKED 		1 0 1 6.7E-02 0 0
CUI: C4022693
Disease: Posteriorly placed anus
Posteriorly placed anus 		1 0 1 6.7E-02 0 0
CUI: C4024068
Disease: Broad distal phalanx of the hallux
Broad distal phalanx of the hallux 		1 0 1 6.7E-02 0 0
CUI: C4275033
Disease: Syndactyly type 1
Syndactyly type 1 		1 0 1 6.7E-02 0 0
CUI: C4305002
Disease: VACTERL syndrome with hydrocephalus
VACTERL syndrome with hydrocephalus 		1 0 1 6.7E-02 0 0