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: C0031925
Disease: Pilonidal Cyst
Pilonidal Cyst 		1 0 1 1.7E-02 0 0
CUI: C0040409
Disease: Tongue Diseases
Tongue Diseases 		1 0 1 1.7E-02 0 0
CUI: C0085222
Disease: Psoas Abscess
Psoas Abscess 		1 0 1 1.7E-02 0 0
CUI: C0154863
Disease: Vitreoretinal dystrophy
Vitreoretinal dystrophy 		1 0 1 1.7E-02 0 0
CUI: C0158651
Disease: Cleft lip, unilateral, complete
Cleft lip, unilateral, complete 		1 0 1 1.7E-02 0 0
CUI: C0238415
Disease: SCLERODERMA, PULMONARY
SCLERODERMA, PULMONARY 		1 0 1 1.7E-02 0 0
CUI: C0241633
Disease: Vaginal dryness
Vaginal dryness 		1 0 1 1.7E-02 0 0
CUI: C0265573
Disease: Phocomelia of upper limb
Phocomelia of upper limb 		1 0 1 1.7E-02 0 0
CUI: C0265843
Disease: Congenital atresia of aortic valve
Congenital atresia of aortic valve 		1 0 1 1.7E-02 0 0
CUI: C0265878
Disease: Preductal coarctation of aorta
Preductal coarctation of aorta 		1 0 1 1.7E-02 0 0
CUI: C0268875
Disease: Urethrorectal fistula
Urethrorectal fistula 		1 0 1 1.7E-02 0 0
CUI: C0270679
Disease: Brain stem herniation
Brain stem herniation 		1 0 1 1.7E-02 0 0
CUI: C0270771
Disease: Syringobulbia
Syringobulbia 		1 0 1 1.7E-02 0 0
CUI: C0279581
Disease: Childhood L2 Acute Lymphoblastic Leukemia
Childhood L2 Acute Lymphoblastic Leukemia 		1 0 1 1.7E-02 0 0
CUI: C0282643
Disease: Smith-Lemli-Opitz Syndrome, Type I
Smith-Lemli-Opitz Syndrome, Type I 		1 0 1 1.7E-02 0 0
CUI: C0282644
Disease: Smith-Lemli-Opitz Syndrome, Type II
Smith-Lemli-Opitz Syndrome, Type II 		1 0 1 1.7E-02 0 0
CUI: C0344787
Disease: Complete atrioventricular septal defect
Complete atrioventricular septal defect 		1 0 1 1.7E-02 0 0
CUI: C0432146
Disease: Supernumerary lumbar vertebra
Supernumerary lumbar vertebra 		1 0 1 1.7E-02 0 0
CUI: C0432238
Disease: Bent bone dysplasia
Bent bone dysplasia 		1 0 1 1.7E-02 0 0
CUI: C0478044
Disease: Other doubling of uterus
Other doubling of uterus 		1 0 1 1.7E-02 0 0
CUI: C0549651
Disease: Abnormality of the lens
Abnormality of the lens 		1 0 1 1.7E-02 0 0
CUI: C0685678
Disease: Incomplete ossification of pubis
Incomplete ossification of pubis 		1 0 1 1.7E-02 0 0
CUI: C0685786
Disease: Cleft mandible
Cleft mandible 		1 0 1 1.7E-02 0 0
CUI: C0741918
Disease: Structural cardiac defects
Structural cardiac defects 		1 0 1 1.7E-02 0 0
CUI: C0795812
Disease: Chromosome 4, trisomy 4q
Chromosome 4, trisomy 4q 		1 0 1 1.7E-02 0 0