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: C0265756
Disease: Congenital atresia of larynx
Congenital atresia of larynx
1 0 1 7.9E-03 0 0
CUI: C0265878
Disease: Preductal coarctation of aorta
Preductal coarctation of aorta
1 0 1 7.9E-03 0 0
CUI: C0266384
Disease: Congenital absence of uterus
Congenital absence of uterus
1 0 1 7.9E-03 0 0
CUI: C0266429
Disease: Monorchism
Monorchism
1 0 1 7.9E-03 0 0
CUI: C0266692
Disease: Craniopagus
Craniopagus
1 0 1 7.9E-03 0 0
CUI: C0267716
Disease: Incisional hernia
Incisional hernia
1 0 1 7.9E-03 0 0
CUI: C0268365
Disease: Marfanoid hypermobility syndrome
Marfanoid hypermobility syndrome
1 0 1 7.9E-03 0 0
CUI: C0268875
Disease: Urethrorectal fistula
Urethrorectal fistula
1 0 1 7.9E-03 0 0
CUI: C0271574
Disease: Empty Sella Syndrome, Primary
Empty Sella Syndrome, Primary
1 0 1 7.9E-03 0 0
CUI: C0277331
Disease: Disease due to Acanthocephala
Disease due to Acanthocephala
1 0 1 7.9E-03 0 0
CUI: C0332778
Disease: Diastasis, Bone
Diastasis, Bone
1 0 1 7.9E-03 0 0
CUI: C0340031
Disease: Mucociliary clearance defect
Mucociliary clearance defect
1 0 1 7.9E-03 0 0
CUI: C0344535
Disease: Congenital corneal opacity
Congenital corneal opacity
1 0 1 7.9E-03 0 0
CUI: C0344987
Disease: Bicuspid pulmonary valve
Bicuspid pulmonary valve
1 0 1 7.9E-03 0 0
CUI: C0345382
Disease: Gorlin Chaudhry Moss syndrome
Gorlin Chaudhry Moss syndrome
1 0 1 7.9E-03 0 0
CUI: C0349477
Disease: Transient neonatal hypothyroidism
Transient neonatal hypothyroidism
1 0 1 7.9E-03 0 0
CUI: C0395905
Disease: Postauricular fistula
Postauricular fistula
1 0 1 7.9E-03 0 0
CUI: C0406716
Disease: Hypodontia and nail dysgenesis
Hypodontia and nail dysgenesis
1 0 1 7.9E-03 0 0
CUI: C0406727
Disease: Orofaciodigital syndrome 4
Orofaciodigital syndrome 4
1 0 1 7.9E-03 0 0
Curly hair-ankyloblepharon-nail dysplasia syndrome
1 0 1 7.9E-03 0 0
CUI: C0409579
Disease: Rheumatic joint disease
Rheumatic joint disease
1 0 1 7.9E-03 0 0
Osteoarthritis of glenohumeral joint
1 0 1 7.9E-03 0 0
CUI: C0431289
Disease: Frontal Encephalocele
Frontal Encephalocele
1 0 1 7.9E-03 0 0
Congenital malformation syndromes involving limbs
1 0 1 7.9E-03 0 0
CUI: C0432125
Disease: Bicoronal craniosynostosis
Bicoronal craniosynostosis
1 0 1 7.9E-03 0 0