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: C0027063
Disease: Myoclonic disorder
Myoclonic disorder 		1 0 1 1.1E-02 0 0
CUI: C0033247
Disease: Proctocolitis
Proctocolitis 		1 0 1 1.1E-02 0 0
CUI: C0034350
Disease: Pyruvate Metabolism, Inborn Errors
Pyruvate Metabolism, Inborn Errors 		1 0 1 1.1E-02 0 0
CUI: C0155002
Disease: Sudden visual loss
Sudden visual loss 		1 0 1 1.1E-02 0 0
CUI: C0268090
Disease: Manganese deficiency
Manganese deficiency 		1 0 1 1.1E-02 0 0
CUI: C0270975
Disease: Infantile encephalopathy AND lactic acidosis
Infantile encephalopathy AND lactic acidosis 		1 0 1 1.1E-02 0 0
CUI: C0423640
Disease: Right Flank Pain
Right Flank Pain 		1 0 1 1.1E-02 0 0
CUI: C1150891
Disease: peptidylamidoglycolate lyase activity
peptidylamidoglycolate lyase activity 		1 0 1 1.1E-02 0 0
CUI: C1266156
Disease: Multicystic mesothelioma, benign
Multicystic mesothelioma, benign 		1 0 1 1.1E-02 0 0
CUI: C1739147
Disease: Subacute necrotising encephalomyopathy
Subacute necrotising encephalomyopathy 		1 0 1 1.1E-02 0 0
CUI: C1824925
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 70
DEAFNESS, AUTOSOMAL RECESSIVE 70 		1 0 1 1.1E-02 0 0
CUI: C1838818
Disease: MUSCLE STIFFNESS, PAINFUL
MUSCLE STIFFNESS, PAINFUL 		1 0 1 1.1E-02 0 0
CUI: C1838868
Disease: Corticospinal tract atrophy
Corticospinal tract atrophy 		1 0 1 1.1E-02 0 0
CUI: C1838876
Disease: MITOCHONDRIAL MYOPATHY, LETHAL, INFANTILE
MITOCHONDRIAL MYOPATHY, LETHAL, INFANTILE 		1 0 1 1.1E-02 0 0
CUI: C1838916
Disease: ATAXIA AND POLYNEUROPATHY, ADULT-ONSET
ATAXIA AND POLYNEUROPATHY, ADULT-ONSET 		1 0 1 1.1E-02 0 0
CUI: C1838954
Disease: STRIATAL NECROSIS, BILATERAL, WITH DYSTONIA
STRIATAL NECROSIS, BILATERAL, WITH DYSTONIA 		1 0 1 1.1E-02 0 0
CUI: C1839022
Disease: Striatonigral Degeneration, Infantile, Mitochondrial
Striatonigral Degeneration, Infantile, Mitochondrial 		1 0 1 1.1E-02 0 0
CUI: C1845095
Disease: DEAFNESS, X-LINKED 5 (disorder)
DEAFNESS, X-LINKED 5 (disorder) 		1 0 1 1.1E-02 0 0
CUI: C1846648
Disease: MICROCEPHALY, AMISH TYPE (disorder)
MICROCEPHALY, AMISH TYPE (disorder) 		1 0 1 1.1E-02 0 0
CUI: C1853202
Disease: PARKINSON DISEASE 13, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO
PARKINSON DISEASE 13, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO 		1 0 1 1.1E-02 0 0
CUI: C1970840
Disease: Leukoencephalopathy With Metaphyseal Chondrodysplasia
Leukoencephalopathy With Metaphyseal Chondrodysplasia 		1 0 1 1.1E-02 0 0
CUI: C1970887
Disease: Abnormal middle ear reflexes
Abnormal middle ear reflexes 		1 0 1 1.1E-02 0 0
CUI: C2584751
Disease: Severe hereditary factor VIII deficiency disease without inhibitor
Severe hereditary factor VIII deficiency disease without inhibitor 		1 0 1 1.1E-02 0 0
CUI: C2677589
Disease: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 9
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 9 		1 0 1 1.1E-02 0 0
CUI: C2931111
Disease: Myopia, susceptibility to
Myopia, susceptibility to 		1 0 1 1.1E-02 0 0