Source: BEFREE ×
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: C0023487
Disease: Acute Promyelocytic Leukemia
Acute Promyelocytic Leukemia 		629 0 68 0.11 0 0
CUI: C1843477
Disease: Epidermolysis Bullosa Simplex Superficialis
Epidermolysis Bullosa Simplex Superficialis 		10 0 6 8.3E-02 0 0
CUI: C0521858
Disease: Decreased drug resistance
Decreased drug resistance 		15 0 6 7.8E-02 0 0
CUI: C0272401
Disease: Virchow's node (disorder)
Virchow's node (disorder) 		30 0 7 7.7E-02 0 0
CUI: C0023524
Disease: Leukoencephalopathy, Progressive Multifocal
Leukoencephalopathy, Progressive Multifocal 		240 0 21 7.3E-02 0 0
CUI: C0267176
Disease: Gastroparesis with diabetes mellitus
Gastroparesis with diabetes mellitus 		20 0 6 7.3E-02 0 0
CUI: C1168327
Disease: High-Grade Prostatic Intraepithelial Neoplasia
High-Grade Prostatic Intraepithelial Neoplasia 		111 0 12 7.2E-02 0 0
CUI: C0263661
Disease: Disorder of skeletal system
Disorder of skeletal system 		25 0 6 6.9E-02 0 0
CUI: C0271694
Disease: Familial partial lipodystrophy
Familial partial lipodystrophy 		25 0 6 6.9E-02 0 0
CUI: C0333440
Disease: Hyaline body
Hyaline body 		11 0 5 6.8E-02 0 0
CUI: C3267047
Disease: Autoimmune necrotizing myopathy
Autoimmune necrotizing myopathy 		11 0 5 6.8E-02 0 0
CUI: C0206693
Disease: Medullary carcinoma
Medullary carcinoma 		75 0 9 6.7E-02 0 0
CUI: C1863843
Disease: Neuronal intranuclear inclusion disease
Neuronal intranuclear inclusion disease 		12 0 5 6.7E-02 0 0
CUI: C0221032
Disease: Familial generalized lipodystrophy
Familial generalized lipodystrophy 		46 0 7 6.5E-02 0 0
CUI: C0206631
Disease: Lipomatous neoplasm
Lipomatous neoplasm 		14 0 5 6.5E-02 0 0
CUI: C1838244
Disease: TIBIAL MUSCULAR DYSTROPHY, TARDIVE
TIBIAL MUSCULAR DYSTROPHY, TARDIVE 		16 0 5 6.3E-02 0 0
CUI: C0432291
Disease: Mandibuloacral dysostosis
Mandibuloacral dysostosis 		17 0 5 6.2E-02 0 0
CUI: C2745900
Disease: Promyelocytic leukemia
Promyelocytic leukemia 		255 0 19 6.2E-02 0 0
CUI: C0752124
Disease: Spinocerebellar Ataxia Type 6 (disorder)
Spinocerebellar Ataxia Type 6 (disorder) 		35 0 6 6.2E-02 0 0
CUI: C4042861
Disease: Obesity, Metabolically Benign
Obesity, Metabolically Benign 		18 0 5 6.2E-02 0 0
CUI: C0085253
Disease: Adult-Onset Still Disease
Adult-Onset Still Disease 		73 0 8 6.0E-02 0 0
CUI: C0039496
Disease: Temporomandibular Joint Dysfunction Syndrome
Temporomandibular Joint Dysfunction Syndrome 		23 0 5 5.8E-02 0 0
CUI: C1368019
Disease: Paget Disease
Paget Disease 		60 0 7 5.8E-02 0 0
CUI: C0238190
Disease: Inclusion Body Myositis (disorder)
Inclusion Body Myositis (disorder) 		79 0 8 5.8E-02 0 0
CUI: C0856053
Disease: Leukemia secondary
Leukemia secondary 		24 0 5 5.7E-02 0 0