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: C0600039
Disease: Urinary outflow obstruction
Urinary outflow obstruction 		1 0 1 1.9E-02 0 0
CUI: C0679360
Disease: Foodborne Disease
Foodborne Disease 		1 0 1 1.9E-02 0 0
CUI: C0679441
Disease: Disorder of olfactory system
Disorder of olfactory system 		1 0 1 1.9E-02 0 0
CUI: C0742115
Disease: Cerebritis
Cerebritis 		1 0 1 1.9E-02 0 0
CUI: C0747149
Disease: Uncontrolled pain
Uncontrolled pain 		1 0 1 1.9E-02 0 0
CUI: C0851882
Disease: Infection caused by Francisella
Infection caused by Francisella 		1 0 1 1.9E-02 0 0
CUI: C0854297
Disease: Head deformity
Head deformity 		1 0 1 1.9E-02 0 0
CUI: C0858727
Disease: Joint swelling inflammatory
Joint swelling inflammatory 		1 0 1 1.9E-02 0 0
CUI: C0859055
Disease: Oedema vascular
Oedema vascular 		1 0 1 1.9E-02 0 0
CUI: C0859389
Disease: DDS syndrome
DDS syndrome 		1 0 1 1.9E-02 0 0
CUI: C1112341
Disease: Connective tissue inflammation
Connective tissue inflammation 		1 0 1 1.9E-02 0 0
CUI: C1167752
Disease: Graft ischaemia
Graft ischaemia 		1 0 1 1.9E-02 0 0
CUI: C1272765
Disease: Minimal deviation adenocarcinoma of endocervical type
Minimal deviation adenocarcinoma of endocervical type 		1 0 1 1.9E-02 0 0
CUI: C1335461
Disease: Postsurgical Stage I Hepatoblastoma
Postsurgical Stage I Hepatoblastoma 		1 0 1 1.9E-02 0 0
CUI: C1541844
Disease: PRESENILE AND SENILE DEMENTIA
PRESENILE AND SENILE DEMENTIA 		1 0 1 1.9E-02 0 0
CUI: C1820738
Disease: Feeding intolerance
Feeding intolerance 		1 0 1 1.9E-02 0 0
CUI: C1832612
Disease: Hypocalcemia, Autosomal Dominant, with Bartter Syndrome
Hypocalcemia, Autosomal Dominant, with Bartter Syndrome 		1 0 1 1.9E-02 0 0
CUI: C1836474
Disease: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7 		1 0 1 1.9E-02 0 0
CUI: C1842444
Disease: AUTOIMMUNE THYROID DISEASE, SUSCEPTIBILITY TO, 3 (finding)
AUTOIMMUNE THYROID DISEASE, SUSCEPTIBILITY TO, 3 (finding) 		1 0 1 1.9E-02 0 0
CUI: C1846331
Disease: Juvenile-onset dystonia
Juvenile-onset dystonia 		1 0 1 1.9E-02 0 0
CUI: C1856697
Disease: Mitochondrial malic enzyme reduced
Mitochondrial malic enzyme reduced 		1 0 1 1.9E-02 0 0
CUI: C1858042
Disease: Becker Nevus Syndrome
Becker Nevus Syndrome 		1 0 1 1.9E-02 0 0
CUI: C1863080
Disease: ALPHA-FETOPROTEIN, HEREDITARY PERSISTENCE OF
ALPHA-FETOPROTEIN, HEREDITARY PERSISTENCE OF 		1 0 1 1.9E-02 0 0
CUI: C1863081
Disease: alpha-Fetoprotein Deficiency
alpha-Fetoprotein Deficiency 		1 0 1 1.9E-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 1.9E-02 0 0