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: C0006262
Disease: Bronchial Fistula
Bronchial Fistula 		1 0 1 9.4E-03 0 0
CUI: C0009761
Disease: Conjunctival Neoplasms
Conjunctival Neoplasms 		1 0 1 9.4E-03 0 0
CUI: C0009765
Disease: Conjunctivitis, Acute Hemorrhagic
Conjunctivitis, Acute Hemorrhagic 		1 0 1 9.4E-03 0 0
CUI: C0025467
Disease: Mesenteric Cyst
Mesenteric Cyst 		1 2 1 9.4E-03 2 1.0E-01
CUI: C0035290
Disease: Reticulohistiocytic granuloma
Reticulohistiocytic granuloma 		1 0 1 9.4E-03 0 0
CUI: C0152190
Disease: Refractive amblyopia
Refractive amblyopia 		1 0 1 9.4E-03 0 0
CUI: C0158564
Disease: Congenital vitreous anomaly
Congenital vitreous anomaly 		1 0 1 9.4E-03 0 0
CUI: C0162164
Disease: Congenital stenosis of pulmonary valve
Congenital stenosis of pulmonary valve 		1 3 1 9.4E-03 1 4.5E-02
CUI: C0162504
Disease: Neutrophilic Eccrine Hidradenitis
Neutrophilic Eccrine Hidradenitis 		1 0 1 9.4E-03 0 0
CUI: C0206619
Disease: Lymphatic Vessel Tumors
Lymphatic Vessel Tumors 		1 2 1 9.4E-03 2 1.0E-01
CUI: C0233283
Disease: Complete breech presentation
Complete breech presentation 		1 1 1 9.4E-03 1 5.0E-02
CUI: C0233286
Disease: Frank Breech Presentation
Frank Breech Presentation 		1 1 1 9.4E-03 1 5.0E-02
CUI: C0235909
Disease: Impaired psychomotor development
Impaired psychomotor development 		1 0 1 9.4E-03 0 0
CUI: C0239894
Disease: HEART DISPLACEMENT
HEART DISPLACEMENT 		1 0 1 9.4E-03 0 0
CUI: C0265833
Disease: Congenital insufficiency of pulmonary valve
Congenital insufficiency of pulmonary valve 		1 1 1 9.4E-03 1 5.0E-02
CUI: C0268357
Disease: Osteogenesis imperfecta, type 1A
Osteogenesis imperfecta, type 1A 		1 0 1 9.4E-03 0 0
CUI: C0278600
Disease: Childhood Brain Stem Glioma
Childhood Brain Stem Glioma 		1 0 1 9.4E-03 0 0
CUI: C0282643
Disease: Smith-Lemli-Opitz Syndrome, Type I
Smith-Lemli-Opitz Syndrome, Type I 		1 0 1 9.4E-03 0 0
CUI: C0282644
Disease: Smith-Lemli-Opitz Syndrome, Type II
Smith-Lemli-Opitz Syndrome, Type II 		1 0 1 9.4E-03 0 0
CUI: C0302323
Disease: Reticulohistiocytosis
Reticulohistiocytosis 		1 0 1 9.4E-03 0 0
CUI: C0340031
Disease: Mucociliary clearance defect
Mucociliary clearance defect 		1 0 1 9.4E-03 0 0
CUI: C0349533
Disease: Lymphoma of intestine
Lymphoma of intestine 		1 0 1 9.4E-03 0 0
CUI: C0398709
Disease: Secretory Component Deficiency
Secretory Component Deficiency 		1 0 1 9.4E-03 0 0
CUI: C0405584
Disease: Sucrose intolerance
Sucrose intolerance 		1 0 1 9.4E-03 0 0
CUI: C0429803
Disease: Bladder trabeculation
Bladder trabeculation 		1 0 1 9.4E-03 0 0