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: C0021355
Disease: Infective otitis externa
Infective otitis externa 		1 0 1 7.1E-02 0 0
CUI: C0152207
Disease: Alternating Exotropia
Alternating Exotropia 		1 0 1 7.1E-02 0 0
CUI: C0157680
Disease: Carbuncle/furuncle
Carbuncle/furuncle 		1 0 1 7.1E-02 0 0
CUI: C0238454
Disease: Cavernous Sinus Thrombosis
Cavernous Sinus Thrombosis 		1 0 1 7.1E-02 0 0
CUI: C0259860
Disease: psychiatric emergencies
psychiatric emergencies 		1 0 1 7.1E-02 0 0
CUI: C0272263
Disease: Cryofibrinogenemia
Cryofibrinogenemia 		1 0 1 7.1E-02 0 0
CUI: C0393968
Disease: Systemic lupus erythematosus encephalitis
Systemic lupus erythematosus encephalitis 		1 0 1 7.1E-02 0 0
CUI: C0477365
Disease: Other specified degenerative diseases of nervous system
Other specified degenerative diseases of nervous system 		1 0 1 7.1E-02 0 0
CUI: C0576690
Disease: Impaired body position sense
Impaired body position sense 		1 0 1 7.1E-02 0 0
CUI: C0578437
Disease: Ischemic foot
Ischemic foot 		1 0 1 7.1E-02 0 0
CUI: C0854328
Disease: Infection due to anaerobic bacteria
Infection due to anaerobic bacteria 		1 0 1 7.1E-02 0 0
CUI: C1302778
Disease: Congenital lymphatic malformation
Congenital lymphatic malformation 		1 0 1 7.1E-02 0 0
CUI: C1827284
Disease: Refractory occipital lobe epilepsy
Refractory occipital lobe epilepsy 		1 0 1 7.1E-02 0 0
CUI: C1834042
Disease: Hypoplasia of facial musculature
Hypoplasia of facial musculature 		1 0 1 7.1E-02 0 0
CUI: C1836439
Disease: Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3 		1 0 1 7.1E-02 0 0
CUI: C1836460
Disease: Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 		1 0 1 7.1E-02 0 0
CUI: C1843852
Disease: SPINOCEREBELLAR ATAXIA WITH EPILEPSY
SPINOCEREBELLAR ATAXIA WITH EPILEPSY 		1 0 1 7.1E-02 0 0
CUI: C1846130
Disease: Mental retardation X-linked, South African type
Mental retardation X-linked, South African type 		1 0 1 7.1E-02 0 0
CUI: C1859863
Disease: Cerebral cortical neurodegeneration
Cerebral cortical neurodegeneration 		1 0 1 7.1E-02 0 0
CUI: C1864668
Disease: Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 4
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 4 		1 0 1 7.1E-02 0 0
CUI: C2349529
Disease: Pneumonia due to methicillin susceptible Staphylococcus aureus
Pneumonia due to methicillin susceptible Staphylococcus aureus 		1 0 1 7.1E-02 0 0
CUI: C2749861
Disease: MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY)
MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY) 		1 0 1 7.1E-02 0 0
CUI: C2751319
Disease: Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5
Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 		1 0 1 7.1E-02 0 0
CUI: C3150172
Disease: MITOCHONDRIAL DNA DEPLETION SYNDROME 8B (MNGIE TYPE)
MITOCHONDRIAL DNA DEPLETION SYNDROME 8B (MNGIE TYPE) 		1 0 1 7.1E-02 0 0
CUI: C3277693
Disease: Punctate vasculitis skin lesions
Punctate vasculitis skin lesions 		1 0 1 7.1E-02 0 0