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: C0009761
Disease: Conjunctival Neoplasms
Conjunctival Neoplasms 		1 0 1 2.0E-02 0 0
CUI: C0015338
Disease: Exstrophy
Exstrophy 		1 0 1 2.0E-02 0 0
CUI: C0030215
Disease: Palatal Neoplasms
Palatal Neoplasms 		1 0 1 2.0E-02 0 0
CUI: C0034184
Disease: Pyelocystitis
Pyelocystitis 		1 0 1 2.0E-02 0 0
CUI: C0035290
Disease: Reticulohistiocytic granuloma
Reticulohistiocytic granuloma 		1 0 1 2.0E-02 0 0
CUI: C0152091
Disease: Osteochondropathy
Osteochondropathy 		1 0 1 2.0E-02 0 0
CUI: C0152190
Disease: Refractive amblyopia
Refractive amblyopia 		1 0 1 2.0E-02 0 0
CUI: C0155477
Disease: Tympanosclerosis involving other combination of structures
Tympanosclerosis involving other combination of structures 		1 0 1 2.0E-02 0 0
CUI: C0158667
Disease: Aplasia of Lacrimal and Salivary Glands
Aplasia of Lacrimal and Salivary Glands 		1 0 1 2.0E-02 0 0
CUI: C0162164
Disease: Congenital stenosis of pulmonary valve
Congenital stenosis of pulmonary valve 		1 0 1 2.0E-02 0 0
CUI: C0162504
Disease: Neutrophilic Eccrine Hidradenitis
Neutrophilic Eccrine Hidradenitis 		1 0 1 2.0E-02 0 0
CUI: C0235410
Disease: Potassium retention
Potassium retention 		1 0 1 2.0E-02 0 0
CUI: C0239894
Disease: HEART DISPLACEMENT
HEART DISPLACEMENT 		1 0 1 2.0E-02 0 0
CUI: C0262477
Disease: Eye problem
Eye problem 		1 0 1 2.0E-02 0 0
CUI: C0264955
Disease: Idiopathic arterial calcification of infancy
Idiopathic arterial calcification of infancy 		1 0 1 2.0E-02 0 0
CUI: C0265701
Disease: Congenital eventration of diaphragm
Congenital eventration of diaphragm 		1 0 1 2.0E-02 0 0
CUI: C0265833
Disease: Congenital insufficiency of pulmonary valve
Congenital insufficiency of pulmonary valve 		1 0 1 2.0E-02 0 0
CUI: C0267716
Disease: Incisional hernia
Incisional hernia 		1 0 1 2.0E-02 0 0
CUI: C0268356
Disease: Osteogenesis imperfecta with blue sclerae AND normal teeth
Osteogenesis imperfecta with blue sclerae AND normal teeth 		1 0 1 2.0E-02 0 0
CUI: C0268365
Disease: Marfanoid hypermobility syndrome
Marfanoid hypermobility syndrome 		1 0 1 2.0E-02 0 0
CUI: C0270250
Disease: Meconium peritonitis
Meconium peritonitis 		1 0 1 2.0E-02 0 0
CUI: C0271618
Disease: Delayed female puberty
Delayed female puberty 		1 0 1 2.0E-02 0 0
CUI: C0278600
Disease: Childhood Brain Stem Glioma
Childhood Brain Stem Glioma 		1 0 1 2.0E-02 0 0
CUI: C0278714
Disease: stage IV Wilms tumor
stage IV Wilms tumor 		1 0 1 2.0E-02 0 0
CUI: C0302323
Disease: Reticulohistiocytosis
Reticulohistiocytosis 		1 0 1 2.0E-02 0 0