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 1.7E-02 0 0
CUI: C0009761
Disease: Conjunctival Neoplasms
Conjunctival Neoplasms 		1 0 1 1.7E-02 0 0
CUI: C0023441
Disease: Leukemia, Experimental
Leukemia, Experimental 		1 0 1 1.7E-02 0 0
CUI: C0030215
Disease: Palatal Neoplasms
Palatal Neoplasms 		1 0 1 1.7E-02 0 0
CUI: C0035290
Disease: Reticulohistiocytic granuloma
Reticulohistiocytic granuloma 		1 0 1 1.7E-02 0 0
CUI: C0152190
Disease: Refractive amblyopia
Refractive amblyopia 		1 0 1 1.7E-02 0 0
CUI: C0153470
Disease: Malignant neoplasm of spleen
Malignant neoplasm of spleen 		1 0 1 1.7E-02 0 0
CUI: C0155477
Disease: Tympanosclerosis involving other combination of structures
Tympanosclerosis involving other combination of structures 		1 0 1 1.7E-02 0 0
CUI: C0158564
Disease: Congenital vitreous anomaly
Congenital vitreous anomaly 		1 0 1 1.7E-02 0 0
CUI: C0162164
Disease: Congenital stenosis of pulmonary valve
Congenital stenosis of pulmonary valve 		1 0 1 1.7E-02 0 0
CUI: C0162504
Disease: Neutrophilic Eccrine Hidradenitis
Neutrophilic Eccrine Hidradenitis 		1 0 1 1.7E-02 0 0
CUI: C0233286
Disease: Frank Breech Presentation
Frank Breech Presentation 		1 0 1 1.7E-02 0 0
CUI: C0235910
Disease: Colagenosis
Colagenosis 		1 0 1 1.7E-02 0 0
CUI: C0239894
Disease: HEART DISPLACEMENT
HEART DISPLACEMENT 		1 0 1 1.7E-02 0 0
CUI: C0264955
Disease: Idiopathic arterial calcification of infancy
Idiopathic arterial calcification of infancy 		1 0 1 1.7E-02 0 0
CUI: C0265273
Disease: Achondrogenesis type 1A
Achondrogenesis type 1A 		1 0 1 1.7E-02 0 0
CUI: C0265729
Disease: Mesatipellic pelvis
Mesatipellic pelvis 		1 0 1 1.7E-02 0 0
CUI: C0265833
Disease: Congenital insufficiency of pulmonary valve
Congenital insufficiency of pulmonary valve 		1 0 1 1.7E-02 0 0
CUI: C0268357
Disease: Osteogenesis imperfecta, type 1A
Osteogenesis imperfecta, type 1A 		1 0 1 1.7E-02 0 0
CUI: C0270250
Disease: Meconium peritonitis
Meconium peritonitis 		1 0 1 1.7E-02 0 0
CUI: C0270920
Disease: Supranuclear paralysis
Supranuclear paralysis 		1 0 1 1.7E-02 0 0
CUI: C0271618
Disease: Delayed female puberty
Delayed female puberty 		1 0 1 1.7E-02 0 0
CUI: C0278600
Disease: Childhood Brain Stem Glioma
Childhood Brain Stem Glioma 		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