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: C0001145
Disease: Acne Keloid
Acne Keloid 		1 0 1 1.8E-02 0 0
CUI: C0006262
Disease: Bronchial Fistula
Bronchial Fistula 		1 0 1 1.8E-02 0 0
CUI: C0037932
Disease: Curvature of spine
Curvature of spine 		1 0 1 1.8E-02 0 0
CUI: C0038834
Disease: Superior Vena Cava Thrombosis
Superior Vena Cava Thrombosis 		1 0 1 1.8E-02 0 0
CUI: C0152091
Disease: Osteochondropathy
Osteochondropathy 		1 0 1 1.8E-02 0 0
CUI: C0152207
Disease: Alternating Exotropia
Alternating Exotropia 		1 0 1 1.8E-02 0 0
CUI: C0153614
Disease: Malignant neoplasm of ureteric orifice
Malignant neoplasm of ureteric orifice 		1 0 1 1.8E-02 0 0
CUI: C0155930
Disease: Tooth Ankylosis
Tooth Ankylosis 		1 0 1 1.8E-02 0 0
CUI: C0158564
Disease: Congenital vitreous anomaly
Congenital vitreous anomaly 		1 0 1 1.8E-02 0 0
CUI: C0162824
Disease: Dermatitis, Photoallergic
Dermatitis, Photoallergic 		1 0 1 1.8E-02 0 0
CUI: C0233286
Disease: Frank Breech Presentation
Frank Breech Presentation 		1 0 1 1.8E-02 0 0
CUI: C0265273
Disease: Achondrogenesis type 1A
Achondrogenesis type 1A 		1 0 1 1.8E-02 0 0
CUI: C0265669
Disease: Congenital dislocation of knee
Congenital dislocation of knee 		1 0 1 1.8E-02 0 0
CUI: C0265905
Disease: Agenesis of pulmonary artery
Agenesis of pulmonary artery 		1 0 1 1.8E-02 0 0
CUI: C0268357
Disease: Osteogenesis imperfecta, type 1A
Osteogenesis imperfecta, type 1A 		1 0 1 1.8E-02 0 0
CUI: C0268474
Disease: Hydroxykynureninuria
Hydroxykynureninuria 		1 0 1 1.8E-02 0 0
CUI: C0271869
Disease: Pseudohypoparathyroidism type I B
Pseudohypoparathyroidism type I B 		1 0 1 1.8E-02 0 0
CUI: C0282643
Disease: Smith-Lemli-Opitz Syndrome, Type I
Smith-Lemli-Opitz Syndrome, Type I 		1 0 1 1.8E-02 0 0
CUI: C0282644
Disease: Smith-Lemli-Opitz Syndrome, Type II
Smith-Lemli-Opitz Syndrome, Type II 		1 0 1 1.8E-02 0 0
CUI: C0332885
Disease: Congenital stenosis
Congenital stenosis 		1 0 1 1.8E-02 0 0
CUI: C0333662
Disease: Hemiatrophy
Hemiatrophy 		1 0 1 1.8E-02 0 0
CUI: C0339352
Disease: Capsular cataract (disorder)
Capsular cataract (disorder) 		1 0 1 1.8E-02 0 0
CUI: C0340031
Disease: Mucociliary clearance defect
Mucociliary clearance defect 		1 0 1 1.8E-02 0 0
CUI: C0342826
Disease: 3-Beta-hydroxy-delta-5-C27-steroid dehydrogenase deficiency
3-Beta-hydroxy-delta-5-C27-steroid dehydrogenase deficiency 		1 0 1 1.8E-02 0 0
CUI: C0344987
Disease: Bicuspid pulmonary valve
Bicuspid pulmonary valve 		1 0 1 1.8E-02 0 0