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 3.6E-02 0 0
CUI: C0002897
Disease: Anemia, Splenic
Anemia, Splenic 		1 0 1 3.6E-02 0 0
CUI: C0022802
Disease: Kuru
Kuru 		1 0 1 3.6E-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 3.6E-02 0 0
CUI: C0233459
Disease: Emotional disorder
Emotional disorder 		1 0 1 3.6E-02 0 0
CUI: C0270958
Disease: Kocher-Debre-Semelaigne syndrome
Kocher-Debre-Semelaigne syndrome 		1 0 1 3.6E-02 0 0
CUI: C0333157
Disease: Colloid Cysts
Colloid Cysts 		1 0 1 3.6E-02 0 0
CUI: C0344787
Disease: Complete atrioventricular septal defect
Complete atrioventricular septal defect 		1 0 1 3.6E-02 0 0
CUI: C0558193
Disease: Stiff limbs
Stiff limbs 		1 0 1 3.6E-02 0 0
CUI: C0576690
Disease: Impaired body position sense
Impaired body position sense 		1 0 1 3.6E-02 0 0
CUI: C0795812
Disease: Chromosome 4, trisomy 4q
Chromosome 4, trisomy 4q 		1 0 1 3.6E-02 0 0
CUI: C0795868
Disease: Chromosome 18, tetrasomy 18p
Chromosome 18, tetrasomy 18p 		1 0 1 3.6E-02 0 0
CUI: C0795939
Disease: AMINOPTERIN SYNDROME SINE AMINOPTERIN
AMINOPTERIN SYNDROME SINE AMINOPTERIN 		1 0 1 3.6E-02 0 0
CUI: C0856836
Disease: Systemic juvenile chronic arthritis
Systemic juvenile chronic arthritis 		1 0 1 3.6E-02 0 0
CUI: C0917967
Disease: Pupillary Functions, Abnormal
Pupillary Functions, Abnormal 		1 0 1 3.6E-02 0 0
CUI: C0948109
Disease: Idiopathic neutropenia
Idiopathic neutropenia 		1 0 1 3.6E-02 0 0
CUI: C1283723
Disease: Deficiency of cathepsin C
Deficiency of cathepsin C 		1 0 1 3.6E-02 0 0
CUI: C1827284
Disease: Refractory occipital lobe epilepsy
Refractory occipital lobe epilepsy 		1 0 1 3.6E-02 0 0
CUI: C1836437
Disease: B-Cell Immunodeficiency, Distal Limb Anomalies, And Urogenital Malformations
B-Cell Immunodeficiency, Distal Limb Anomalies, And Urogenital Malformations 		1 0 1 3.6E-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 3.6E-02 0 0
CUI: C1843815
Disease: Newfoundland Rod-Cone Dystrophy
Newfoundland Rod-Cone Dystrophy 		1 0 1 3.6E-02 0 0
CUI: C1843816
Disease: Bothnia Retinal Dystrophy
Bothnia Retinal Dystrophy 		1 0 1 3.6E-02 0 0
CUI: C1843852
Disease: SPINOCEREBELLAR ATAXIA WITH EPILEPSY
SPINOCEREBELLAR ATAXIA WITH EPILEPSY 		1 2 1 3.6E-02 2 1.6E-02
CUI: C1847650
Disease: SPONGIFORM ENCEPHALOPATHY WITH NEUROPSYCHIATRIC FEATURES
SPONGIFORM ENCEPHALOPATHY WITH NEUROPSYCHIATRIC FEATURES 		1 0 1 3.6E-02 0 0
CUI: C1850407
Disease: Navajo Familial Neurogenic Arthropathy
Navajo Familial Neurogenic Arthropathy 		1 0 1 3.6E-02 0 0