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: C4748752
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 3
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 3 		1 0 1 2.8E-02 0 0
CUI: C4748753
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 4
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 4 		1 0 1 2.8E-02 0 0
CUI: C4748754
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 5
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 5 		1 0 1 2.8E-02 0 0
CUI: C4748766
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 8
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 8 		1 0 1 2.8E-02 0 0
CUI: C4748770
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 13
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 13 		1 0 1 2.8E-02 0 0
CUI: C4748791
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 19
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 19 		1 0 1 2.8E-02 0 0
CUI: C4748796
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 22
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 22 		1 0 1 2.8E-02 0 0
CUI: C4748799
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 23
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 23 		1 0 1 2.8E-02 0 0
CUI: C4748809
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 26
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 26 		1 0 1 2.8E-02 0 0
CUI: C0334416
Disease: Parasympathetic paraganglioma
Parasympathetic paraganglioma 		2 0 1 2.7E-02 0 0
CUI: C0375362
Disease: Peritoneal adhesions (postoperative) (postinfection)
Peritoneal adhesions (postoperative) (postinfection) 		2 0 1 2.7E-02 0 0
CUI: C0741270
Disease: Intermittent ataxia
Intermittent ataxia 		2 0 1 2.7E-02 0 0
CUI: C0751595
Disease: Juvenile Pyruvate Dehydrogenase Complex Deficiency Disease
Juvenile Pyruvate Dehydrogenase Complex Deficiency Disease 		2 0 1 2.7E-02 0 0
CUI: C0751596
Disease: Pyruvate Dehydrogenase Complex Deficiency Disease, Neonatal
Pyruvate Dehydrogenase Complex Deficiency Disease, Neonatal 		2 0 1 2.7E-02 0 0
CUI: C0751597
Disease: Ataxia with Lactic Acidosis, Type I
Ataxia with Lactic Acidosis, Type I 		2 0 1 2.7E-02 0 0
CUI: C0919785
Disease: Decreased transferrin saturation
Decreased transferrin saturation 		2 0 1 2.7E-02 0 0
CUI: C1843807
Disease: Basal ganglia disease, biotin-responsive
Basal ganglia disease, biotin-responsive 		2 0 1 2.7E-02 0 0
CUI: C1848097
Disease: Spondyloepimetaphyseal Dysplasia, X-Linked
Spondyloepimetaphyseal Dysplasia, X-Linked 		2 0 1 2.7E-02 0 0
CUI: C1864002
Disease: GRACILE SYNDROME (disorder)
GRACILE SYNDROME (disorder) 		2 0 1 2.7E-02 0 0
CUI: C2749864
Disease: MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)
MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA) 		2 0 1 2.7E-02 0 0
CUI: C2751843
Disease: Leukoencephalopathy, Cystic, Without Megalencephaly
Leukoencephalopathy, Cystic, Without Megalencephaly 		2 0 1 2.7E-02 0 0
CUI: C3541471
Disease: MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1 		2 0 2 5.6E-02 0 0
CUI: C3554534
Disease: CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 2
CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 2 		2 0 1 2.7E-02 0 0
CUI: C3711369
Disease: Succinate-Coa Ligase Deficiency
Succinate-Coa Ligase Deficiency 		2 0 2 5.6E-02 0 0
CUI: C3806306
Disease: Periarticular subcutaneous nodules
Periarticular subcutaneous nodules 		2 0 1 2.7E-02 0 0