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: C0033247
Disease: Proctocolitis
Proctocolitis 		1 0 1 3.1E-02 0 0
CUI: C0155241
Disease: Lacrimal mucocele
Lacrimal mucocele 		1 0 1 3.1E-02 0 0
CUI: C0232874
Disease: Febrile proteinuria
Febrile proteinuria 		1 0 1 3.1E-02 0 0
CUI: C0266445
Disease: Congenital atresia of vas deferens
Congenital atresia of vas deferens 		1 0 1 3.1E-02 0 0
CUI: C0268486
Disease: Hereditary hypertyrosinemia
Hereditary hypertyrosinemia 		1 0 1 3.1E-02 0 0
CUI: C0270975
Disease: Infantile encephalopathy AND lactic acidosis
Infantile encephalopathy AND lactic acidosis 		1 0 1 3.1E-02 0 0
CUI: C0679254
Disease: Disease recurrence
Disease recurrence 		1 0 1 3.1E-02 0 0
CUI: C0857576
Disease: Abnormality of thyroid physiology
Abnormality of thyroid physiology 		1 0 1 3.1E-02 0 0
CUI: C1266156
Disease: Multicystic mesothelioma, benign
Multicystic mesothelioma, benign 		1 0 1 3.1E-02 0 0
CUI: C1567427
Disease: Bilateral Multicystic Dysplastic Kidneys
Bilateral Multicystic Dysplastic Kidneys 		1 0 1 3.1E-02 0 0
CUI: C1622439
Disease: Lentiglobus
Lentiglobus 		1 0 1 3.1E-02 0 0
CUI: C1735903
Disease: Chronic acidosis
Chronic acidosis 		1 0 1 3.1E-02 0 0
CUI: C1835612
Disease: LACRIMAL DUCT DEFECT
LACRIMAL DUCT DEFECT 		1 0 1 3.1E-02 0 0
CUI: C1846349
Disease: Impaired reabsorption of chloride
Impaired reabsorption of chloride 		1 0 1 3.1E-02 0 0
CUI: C1848695
Disease: Episodic peripheral neuropathy
Episodic peripheral neuropathy 		1 0 1 3.1E-02 0 0
CUI: C1860118
Disease: Acrofrontofacionasal dysostosis syndrome
Acrofrontofacionasal dysostosis syndrome 		1 0 1 3.1E-02 0 0
CUI: C1864669
Disease: NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCY
NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCY 		1 0 1 3.1E-02 0 0
CUI: C1864670
Disease: Neuronal Ceroid Lipofuscinosis, Congenital
Neuronal Ceroid Lipofuscinosis, Congenital 		1 0 1 3.1E-02 0 0
CUI: C2584751
Disease: Severe hereditary factor VIII deficiency disease without inhibitor
Severe hereditary factor VIII deficiency disease without inhibitor 		1 0 1 3.1E-02 0 0
CUI: C2676786
Disease: Nephrolithiasis-Osteoporosis, Hypophosphatemic, 1
Nephrolithiasis-Osteoporosis, Hypophosphatemic, 1 		1 0 1 3.1E-02 0 0
CUI: C2713392
Disease: Phosphatidylinositol 4,5-Bisphosphate 5-Phosphatase Deficiency
Phosphatidylinositol 4,5-Bisphosphate 5-Phosphatase Deficiency 		1 0 1 3.1E-02 0 0
CUI: C2749685
Disease: CYSTINOSIS, ATYPICAL NEPHROPATHIC (disorder)
CYSTINOSIS, ATYPICAL NEPHROPATHIC (disorder) 		1 0 1 3.1E-02 0 0
CUI: C2931013
Disease: Cystinosis, benign, nonnephropathic
Cystinosis, benign, nonnephropathic 		1 0 1 3.1E-02 0 0
CUI: C3150652
Disease: FANCONI RENOTUBULAR SYNDROME 2
FANCONI RENOTUBULAR SYNDROME 2 		1 0 1 3.1E-02 0 0
CUI: C3151975
Disease: DEAFNESS, SENSORINEURAL, WITH NEUROLOGIC FEATURES
DEAFNESS, SENSORINEURAL, WITH NEUROLOGIC FEATURES 		1 0 1 3.1E-02 0 0