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: C0265248
Disease: Ruvalcaba Syndrome
Ruvalcaba Syndrome
1 0 1 4.3E-03 0 0
CUI: C0265404
Disease: 4q partial monosomy syndrome
4q partial monosomy syndrome
1 0 1 4.3E-03 0 0
CUI: C0265878
Disease: Preductal coarctation of aorta
Preductal coarctation of aorta
1 0 1 4.3E-03 0 0
CUI: C0265974
Disease: Birthmark
Birthmark
1 0 1 4.3E-03 0 0
CUI: C0266094
Disease: Congenital macrocheilia
Congenital macrocheilia
1 0 1 4.3E-03 0 0
Congenital obstruction of bladder neck
1 0 1 4.3E-03 0 0
CUI: C0266384
Disease: Congenital absence of uterus
Congenital absence of uterus
1 0 1 4.3E-03 0 0
CUI: C0266692
Disease: Craniopagus
Craniopagus
1 0 1 4.3E-03 0 0
CUI: C0266878
Disease: External resorption of tooth
External resorption of tooth
1 0 1 4.3E-03 0 0
CUI: C0267024
Disease: Hypertrophy of lip
Hypertrophy of lip
1 0 1 4.3E-03 0 0
CUI: C0267095
Disease: Leukoplakia of esophagus
Leukoplakia of esophagus
1 0 1 4.3E-03 0 0
CUI: C0267581
Disease: Rectal Stenosis
Rectal Stenosis
1 0 1 4.3E-03 0 0
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis
1 0 1 4.3E-03 0 0
CUI: C0268357
Disease: Osteogenesis imperfecta, type 1A
Osteogenesis imperfecta, type 1A
1 0 1 4.3E-03 0 0
CUI: C0268875
Disease: Urethrorectal fistula
Urethrorectal fistula
1 0 1 4.3E-03 0 0
CUI: C0268889
Disease: Prostatic Obstruction
Prostatic Obstruction
1 0 1 4.3E-03 0 0
CUI: C0271198
Disease: Scotoma, Arcuate
Scotoma, Arcuate
1 0 1 4.3E-03 0 0
CUI: C0271574
Disease: Empty Sella Syndrome, Primary
Empty Sella Syndrome, Primary
1 0 1 4.3E-03 0 0
Hyperparathyroidism due to vitamin D deficiency
1 0 1 4.3E-03 0 0
CUI: C0276270
Disease: Oral papillomatosis
Oral papillomatosis
1 0 1 4.3E-03 0 0
CUI: C0278513
Disease: Stage IIIB Breast Carcinoma
Stage IIIB Breast Carcinoma
1 0 1 4.3E-03 0 0
CUI: C0279602
Disease: Fibroblastic osteosarcoma
Fibroblastic osteosarcoma
1 0 1 4.3E-03 0 0
salivary gland squamous cell carcinoma
1 0 1 4.3E-03 0 0
Squamous cell carcinoma of the nasal cavity
1 0 1 4.3E-03 0 0
CUI: C0282643
Disease: Smith-Lemli-Opitz Syndrome, Type I
Smith-Lemli-Opitz Syndrome, Type I
1 0 1 4.3E-03 0 0