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: C0003910
Disease: Articulation Disorders
Articulation Disorders 		1 0 1 2.5E-02 0 0
CUI: C0010334
Disease: Crisscross Heart
Crisscross Heart 		1 0 1 2.5E-02 0 0
CUI: C0024950
Disease: Maxillary Diseases
Maxillary Diseases 		1 0 1 2.5E-02 0 0
CUI: C0026683
Disease: Mucocele
Mucocele 		1 0 1 2.5E-02 0 0
CUI: C0029437
Disease: Idiopathic Multicentric Osteolyses
Idiopathic Multicentric Osteolyses 		1 0 1 2.5E-02 0 0
CUI: C0152190
Disease: Refractive amblyopia
Refractive amblyopia 		1 0 1 2.5E-02 0 0
CUI: C0154089
Disease: Carcinoma in situ of penis
Carcinoma in situ of penis 		1 0 1 2.5E-02 0 0
CUI: C0155100
Disease: Peripheral opacity of cornea
Peripheral opacity of cornea 		1 0 1 2.5E-02 0 0
CUI: C0155477
Disease: Tympanosclerosis involving other combination of structures
Tympanosclerosis involving other combination of structures 		1 0 1 2.5E-02 0 0
CUI: C0162164
Disease: Congenital stenosis of pulmonary valve
Congenital stenosis of pulmonary valve 		1 3 1 2.5E-02 1 0.14
CUI: C0232259
Disease: Mid-systolic murmur
Mid-systolic murmur 		1 0 1 2.5E-02 0 0
CUI: C0233483
Disease: Free-floating anxiety
Free-floating anxiety 		1 0 1 2.5E-02 0 0
CUI: C0235204
Disease: Irrational thoughts
Irrational thoughts 		1 0 1 2.5E-02 0 0
CUI: C0239894
Disease: HEART DISPLACEMENT
HEART DISPLACEMENT 		1 0 1 2.5E-02 0 0
CUI: C0262477
Disease: Eye problem
Eye problem 		1 0 1 2.5E-02 0 0
CUI: C0264954
Disease: Arteriovascular degeneration
Arteriovascular degeneration 		1 0 1 2.5E-02 0 0
CUI: C0264955
Disease: Idiopathic arterial calcification of infancy
Idiopathic arterial calcification of infancy 		1 0 1 2.5E-02 0 0
CUI: C0265833
Disease: Congenital insufficiency of pulmonary valve
Congenital insufficiency of pulmonary valve 		1 1 1 2.5E-02 1 0.20
CUI: C0267548
Disease: Ileocolic intussusception
Ileocolic intussusception 		1 0 1 2.5E-02 0 0
CUI: C0268288
Disease: Mild steroid 21-hydroxylase deficiency
Mild steroid 21-hydroxylase deficiency 		1 0 1 2.5E-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 2.5E-02 0 0
CUI: C0270250
Disease: Meconium peritonitis
Meconium peritonitis 		1 0 1 2.5E-02 0 0
CUI: C0272080
Disease: Hemoglobin D disease
Hemoglobin D disease 		1 0 1 2.5E-02 0 0
CUI: C0278714
Disease: stage IV Wilms tumor
stage IV Wilms tumor 		1 0 1 2.5E-02 0 0
CUI: C0332881
Disease: Congenital pseudoarthrosis
Congenital pseudoarthrosis 		1 0 1 2.5E-02 0 0