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: C0001889
Disease: Akinetic Mutism
Akinetic Mutism 		1 0 1 5.0E-02 0 0
CUI: C0007761
Disease: Myoclonic Cerebellar Dyssynergia
Myoclonic Cerebellar Dyssynergia 		1 0 1 5.0E-02 0 0
CUI: C0017409
Disease: Herpes Zoster Oticus
Herpes Zoster Oticus 		1 0 1 5.0E-02 0 0
CUI: C0022802
Disease: Kuru
Kuru 		1 0 1 5.0E-02 0 0
CUI: C0155379
Disease: Nystagmus associated with disorder of the vestibular system
Nystagmus associated with disorder of the vestibular system 		1 0 1 5.0E-02 0 0
CUI: C0333157
Disease: Colloid Cysts
Colloid Cysts 		1 0 1 5.0E-02 0 0
CUI: C0338464
Disease: Epilepsy co-occurrent and due to dementia
Epilepsy co-occurrent and due to dementia 		1 0 1 5.0E-02 0 0
CUI: C0747733
Disease: Polychondritis
Polychondritis 		1 0 1 5.0E-02 0 0
CUI: C0795927
Disease: Deafness, congenital onychodystrophy, recessive form
Deafness, congenital onychodystrophy, recessive form 		1 0 1 5.0E-02 0 0
CUI: C0917967
Disease: Pupillary Functions, Abnormal
Pupillary Functions, Abnormal 		1 0 1 5.0E-02 0 0
CUI: C1272765
Disease: Minimal deviation adenocarcinoma of endocervical type
Minimal deviation adenocarcinoma of endocervical type 		1 0 1 5.0E-02 0 0
CUI: C1333446
Disease: Esophageal Gastrointestinal Stromal Tumor
Esophageal Gastrointestinal Stromal Tumor 		1 0 1 5.0E-02 0 0
CUI: C1378512
Disease: Blast cell leukemia
Blast cell leukemia 		1 0 1 5.0E-02 0 0
CUI: C1834580
Disease: MYOCLONUS AND ATAXIA
MYOCLONUS AND ATAXIA 		1 0 1 5.0E-02 0 0
CUI: C1837510
Disease: Progressive loss of facial adipose tissue
Progressive loss of facial adipose tissue 		1 0 1 5.0E-02 0 0
CUI: C1842531
Disease: Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp
Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp 		1 0 1 5.0E-02 0 0
CUI: C1847650
Disease: SPONGIFORM ENCEPHALOPATHY WITH NEUROPSYCHIATRIC FEATURES
SPONGIFORM ENCEPHALOPATHY WITH NEUROPSYCHIATRIC FEATURES 		1 0 1 5.0E-02 0 0
CUI: C1849151
Disease: Hypermyelinated retinal nerve fibers
Hypermyelinated retinal nerve fibers 		1 0 1 5.0E-02 0 0
CUI: C1849152
Disease: Swan neck-like deformities of the fingers
Swan neck-like deformities of the fingers 		1 0 1 5.0E-02 0 0
CUI: C1856275
Disease: Glycoprotein Storage Disease
Glycoprotein Storage Disease 		1 0 1 5.0E-02 0 0
CUI: C1856476
Disease: Gaucher Disease, Type Iiic
Gaucher Disease, Type Iiic 		1 0 1 5.0E-02 0 0
CUI: C1856478
Disease: Hypometric horizontal saccades
Hypometric horizontal saccades 		1 0 1 5.0E-02 0 0
CUI: C1864112
Disease: HUNTINGTON DISEASE-LIKE 1
HUNTINGTON DISEASE-LIKE 1 		1 0 1 5.0E-02 0 0
CUI: C1969957
Disease: Creutzfeldt-Jakob Disease, Heidenhain Variant
Creutzfeldt-Jakob Disease, Heidenhain Variant 		1 0 1 5.0E-02 0 0
CUI: C2316460
Disease: Pseudobulbar affect
Pseudobulbar affect 		1 0 1 5.0E-02 0 0