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: C4024693
Disease: Factor X activation deficiency
Factor X activation deficiency 		1 0 1 6.7E-02 0 0
CUI: C4025048
Disease: Elongated radius
Elongated radius 		1 0 1 6.7E-02 0 0
CUI: C4310712
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43 		1 0 1 6.7E-02 0 0
CUI: C0001364
Disease: Massive Hepatic Necrosis
Massive Hepatic Necrosis 		2 0 1 6.2E-02 0 0
CUI: C0403548
Disease: Salcedo syndrome
Salcedo syndrome 		2 0 1 6.2E-02 0 0
CUI: C1834384
Disease: Glenoid fossa hypoplasia
Glenoid fossa hypoplasia 		2 0 1 6.2E-02 0 0
CUI: C1862391
Disease: ASD I
ASD I 		2 0 1 6.2E-02 0 0
CUI: C1862392
Disease: Atrial Septal Defect, Secundum Type
Atrial Septal Defect, Secundum Type 		2 0 1 6.2E-02 0 0
CUI: C1862393
Disease: ASD II
ASD II 		2 0 1 6.2E-02 0 0
CUI: C3810170
Disease: DEAFNESS, AUTOSOMAL DOMINANT 56
DEAFNESS, AUTOSOMAL DOMINANT 56 		2 0 1 6.2E-02 0 0
CUI: C4021695
Disease: Hypoplastic radial head
Hypoplastic radial head 		2 0 1 6.2E-02 0 0
CUI: C0451693
Disease: Severe combined immunodeficiency with low T- and B-cell numbers
Severe combined immunodeficiency with low T- and B-cell numbers 		3 0 1 5.9E-02 0 0
CUI: C1834386
Disease: Hypoplasia of first ribs
Hypoplasia of first ribs 		3 0 1 5.9E-02 0 0
CUI: C1853566
Disease: Genitopatellar Syndrome
Genitopatellar Syndrome 		3 0 1 5.9E-02 0 0
CUI: C1865370
Disease: Severe combined immunodeficiency with sensitivity to ionizing radiation
Severe combined immunodeficiency with sensitivity to ionizing radiation 		3 0 1 5.9E-02 0 0
CUI: C0004331
Disease: Auriculo-Ventricular Dissociation
Auriculo-Ventricular Dissociation 		4 0 1 5.6E-02 0 0
CUI: C0264641
Disease: Endocrine hypertension
Endocrine hypertension 		4 0 1 5.6E-02 0 0
CUI: C0343730
Disease: Perianal warts
Perianal warts 		4 0 1 5.6E-02 0 0
CUI: C0349555
Disease: Vaginal intraepithelial neoplasia grade 2
Vaginal intraepithelial neoplasia grade 2 		4 0 1 5.6E-02 0 0
CUI: C0751774
Disease: Nocturnal Myoclonus Syndrome
Nocturnal Myoclonus Syndrome 		4 0 1 5.6E-02 0 0
CUI: C1832322
Disease: Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, NK Cell-Positive
Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, NK Cell-Positive 		4 0 1 5.6E-02 0 0
CUI: C2910126
Disease: Patent or persistent ostium secundum defect (type II)
Patent or persistent ostium secundum defect (type II) 		4 0 1 5.6E-02 0 0
CUI: C2910127
Disease: Patent or persistent sinus venosus defect
Patent or persistent sinus venosus defect 		4 0 1 5.6E-02 0 0
CUI: C3714697
Disease: AV Block Second Degree by ECG Finding
AV Block Second Degree by ECG Finding 		4 0 1 5.6E-02 0 0
CUI: C4023501
Disease: Focal myoclonic seizures
Focal myoclonic seizures 		4 0 1 5.6E-02 0 0