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: C0042907
Disease: Vitreous Detachment
Vitreous Detachment 		1 0 1 6.2E-02 0 0
CUI: C0242036
Disease: Paraplegia, Ataxic
Paraplegia, Ataxic 		1 0 1 6.2E-02 0 0
CUI: C0262477
Disease: Eye problem
Eye problem 		1 0 1 6.2E-02 0 0
CUI: C0278114
Disease: Paraplegia, Cerebral
Paraplegia, Cerebral 		1 0 1 6.2E-02 0 0
CUI: C0278115
Disease: Paraplegia, Spinal
Paraplegia, Spinal 		1 0 1 6.2E-02 0 0
CUI: C0278714
Disease: stage IV Wilms tumor
stage IV Wilms tumor 		1 0 1 6.2E-02 0 0
CUI: C0334454
Disease: Dermatofibrosarcoma Protuberans, Myxoid
Dermatofibrosarcoma Protuberans, Myxoid 		1 0 1 6.2E-02 0 0
CUI: C0452143
Disease: Paraplegia, Flaccid
Paraplegia, Flaccid 		1 0 1 6.2E-02 0 0
CUI: C0521668
Disease: Primary Thunderclap Headache
Primary Thunderclap Headache 		1 0 1 6.2E-02 0 0
CUI: C0524679
Disease: Neuropapillitis
Neuropapillitis 		1 0 1 6.2E-02 0 0
CUI: C0685661
Disease: Congenital anomaly of ischium
Congenital anomaly of ischium 		1 0 1 6.2E-02 0 0
CUI: C0796036
Disease: Marinesco-Sjogren-like syndrome (MSLS)
Marinesco-Sjogren-like syndrome (MSLS) 		1 0 1 6.2E-02 0 0
CUI: C0856900
Disease: Sarcoma of skin
Sarcoma of skin 		1 0 1 6.2E-02 0 0
CUI: C1827284
Disease: Refractory occipital lobe epilepsy
Refractory occipital lobe epilepsy 		1 0 1 6.2E-02 0 0
CUI: C1843852
Disease: SPINOCEREBELLAR ATAXIA WITH EPILEPSY
SPINOCEREBELLAR ATAXIA WITH EPILEPSY 		1 2 1 6.2E-02 1 0.14
CUI: C1854488
Disease: Spinocerebellar ataxia 13
Spinocerebellar ataxia 13 		1 0 1 6.2E-02 0 0
CUI: C1856231
Disease: Thin calvarium
Thin calvarium 		1 0 1 6.2E-02 0 0
CUI: C1859863
Disease: Cerebral cortical neurodegeneration
Cerebral cortical neurodegeneration 		1 0 1 6.2E-02 0 0
CUI: C1866182
Disease: Penttinen-Aula syndrome
Penttinen-Aula syndrome 		1 0 1 6.2E-02 0 0
CUI: C1968845
Disease: Primary Lateral Sclerosis, Adult, 1
Primary Lateral Sclerosis, Adult, 1 		1 0 1 6.2E-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 6.2E-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 6.2E-02 0 0
CUI: C2751807
Disease: Emery-Dreifuss Muscular Dystrophy 4
Emery-Dreifuss Muscular Dystrophy 4 		1 0 1 6.2E-02 0 0
CUI: C2828721
Disease: SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE 		1 0 1 6.2E-02 0 0
CUI: C3150172
Disease: MITOCHONDRIAL DNA DEPLETION SYNDROME 8B (MNGIE TYPE)
MITOCHONDRIAL DNA DEPLETION SYNDROME 8B (MNGIE TYPE) 		1 0 1 6.2E-02 0 0