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: C0236124
Disease: Gastrointestinal obstruction
Gastrointestinal obstruction 		1 0 1 0.14 0 0
CUI: C0344787
Disease: Complete atrioventricular septal defect
Complete atrioventricular septal defect 		1 0 1 0.14 0 0
CUI: C0795812
Disease: Chromosome 4, trisomy 4q
Chromosome 4, trisomy 4q 		1 0 1 0.14 0 0
CUI: C0795868
Disease: Chromosome 18, tetrasomy 18p
Chromosome 18, tetrasomy 18p 		1 0 1 0.14 0 0
CUI: C0795939
Disease: AMINOPTERIN SYNDROME SINE AMINOPTERIN
AMINOPTERIN SYNDROME SINE AMINOPTERIN 		1 0 1 0.14 0 0
CUI: C2930922
Disease: Reginato Schiapachasse syndrome
Reginato Schiapachasse syndrome 		1 0 1 0.14 0 0
CUI: C4512053
Disease: 4p16.3 microduplication syndrome
4p16.3 microduplication syndrome 		1 0 1 0.14 0 0
CUI: C4520921
Disease: Stage 0 Gastric Cancer AJCC v6 and v7
Stage 0 Gastric Cancer AJCC v6 and v7 		1 0 1 0.14 0 0
CUI: C4539937
Disease: JOUBERT SYNDROME 30
JOUBERT SYNDROME 30 		1 0 1 0.14 0 0
CUI: C4551654
Disease: Altman type IV sacrococcygeal teratoma
Altman type IV sacrococcygeal teratoma 		1 0 1 0.14 0 0
CUI: C4707448
Disease: Ring chromosome 2 syndrome
Ring chromosome 2 syndrome 		1 0 1 0.14 0 0
CUI: C0178703
Disease: Hypertrophic osteoarthropathy
Hypertrophic osteoarthropathy 		2 0 1 0.12 0 0
CUI: C0263538
Disease: Clubbing of nail
Clubbing of nail 		2 0 1 0.12 0 0
CUI: C0265931
Disease: Persistent left superior vena cava
Persistent left superior vena cava 		2 0 1 0.12 0 0
CUI: C0277792
Disease: Pathognomonic sign
Pathognomonic sign 		2 0 1 0.12 0 0
CUI: C0302246
Disease: Hexadactyly
Hexadactyly 		2 0 1 0.12 0 0
CUI: C0345408
Disease: Hereditary clubbing
Hereditary clubbing 		2 0 1 0.12 0 0
CUI: C0431415
Disease: Lumbosacral agenesis
Lumbosacral agenesis 		2 0 1 0.12 0 0
CUI: C0431943
Disease: Lower Extremity Deformities, Congenital
Lower Extremity Deformities, Congenital 		2 0 1 0.12 0 0
CUI: C0795805
Disease: Chromosome 2, trisomy 2q
Chromosome 2, trisomy 2q 		2 0 1 0.12 0 0
CUI: C1332582
Disease: Primary bone lymphoma
Primary bone lymphoma 		2 0 1 0.12 0 0
CUI: C1409412
Disease: Periostosis
Periostosis 		2 0 1 0.12 0 0
CUI: C1838568
Disease: Sacral defect and anterior sacral meningocele
Sacral defect and anterior sacral meningocele 		2 0 1 0.12 0 0
CUI: C1838569
Disease: Caudal Dysgenesis Syndrome
Caudal Dysgenesis Syndrome 		2 0 1 0.12 0 0
CUI: C1842464
Disease: Nablus mask-like facial syndrome
Nablus mask-like facial syndrome 		2 0 1 0.12 0 0