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: C0034350
Disease: Pyruvate Metabolism, Inborn Errors
Pyruvate Metabolism, Inborn Errors 		1 0 1 8.3E-02 0 0
CUI: C0235055
Disease: Skeletal muscle paralysis
Skeletal muscle paralysis 		1 0 1 8.3E-02 0 0
CUI: C0275616
Disease: Infection due to Clostridium chauvoei
Infection due to Clostridium chauvoei 		1 0 1 8.3E-02 0 0
CUI: C0742608
Disease: colon (non-specific) polyp hyperplastic
colon (non-specific) polyp hyperplastic 		1 0 1 8.3E-02 0 0
CUI: C0751898
Disease: Tic, Gestural
Tic, Gestural 		1 0 1 8.3E-02 0 0
CUI: C0751899
Disease: Tic, Transient
Tic, Transient 		1 0 1 8.3E-02 0 0
CUI: C0854069
Disease: Tumor pain
Tumor pain 		1 0 1 8.3E-02 0 0
CUI: C0858547
Disease: Neuroparalysis
Neuroparalysis 		1 0 1 8.3E-02 0 0
CUI: C1834703
Disease: Neuropathy, Distal Hereditary Motor, Type VIIA
Neuropathy, Distal Hereditary Motor, Type VIIA 		1 0 1 8.3E-02 0 0
CUI: C1853949
Disease: MYASTHENIA, FAMILIAL INFANTILE, 1
MYASTHENIA, FAMILIAL INFANTILE, 1 		1 0 1 8.3E-02 0 0
CUI: C3808739
Disease: MYASTHENIC SYNDROME, CONGENITAL, 8
MYASTHENIC SYNDROME, CONGENITAL, 8 		1 0 1 8.3E-02 0 0
CUI: C4225235
Disease: MYASTHENIC SYNDROME, CONGENITAL, 19
MYASTHENIC SYNDROME, CONGENITAL, 19 		1 0 1 8.3E-02 0 0
CUI: C4310694
Disease: MYASTHENIC SYNDROME, CONGENITAL, 20, PRESYNAPTIC
MYASTHENIC SYNDROME, CONGENITAL, 20, PRESYNAPTIC 		1 0 1 8.3E-02 0 0
CUI: C4476566
Disease: Abnormal brain choline level by MRS
Abnormal brain choline level by MRS 		1 0 1 8.3E-02 0 0
CUI: C4748678
Disease: MYASTHENIC SYNDROME, CONGENITAL, 23, PRESYNAPTIC
MYASTHENIC SYNDROME, CONGENITAL, 23, PRESYNAPTIC 		1 0 1 8.3E-02 0 0
CUI: C4748684
Disease: MYASTHENIC SYNDROME, CONGENITAL, 24, PRESYNAPTIC
MYASTHENIC SYNDROME, CONGENITAL, 24, PRESYNAPTIC 		1 0 1 8.3E-02 0 0
CUI: C0393929
Disease: Familial infantile myasthenia
Familial infantile myasthenia 		2 0 2 0.17 0 0
CUI: C0741270
Disease: Intermittent ataxia
Intermittent ataxia 		2 0 1 7.7E-02 0 0
CUI: C0751595
Disease: Juvenile Pyruvate Dehydrogenase Complex Deficiency Disease
Juvenile Pyruvate Dehydrogenase Complex Deficiency Disease 		2 0 1 7.7E-02 0 0
CUI: C0751596
Disease: Pyruvate Dehydrogenase Complex Deficiency Disease, Neonatal
Pyruvate Dehydrogenase Complex Deficiency Disease, Neonatal 		2 0 1 7.7E-02 0 0
CUI: C0751597
Disease: Ataxia with Lactic Acidosis, Type I
Ataxia with Lactic Acidosis, Type I 		2 0 1 7.7E-02 0 0
CUI: C0752251
Disease: Muscle Disease Manifestations
Muscle Disease Manifestations 		2 0 1 7.7E-02 0 0
CUI: C1834015
Disease: Progressive ptosis
Progressive ptosis 		2 0 1 7.7E-02 0 0
CUI: C1853950
Disease: Generalized hypotonia due to defect at the neuromuscular junction
Generalized hypotonia due to defect at the neuromuscular junction 		2 0 2 0.17 0 0
CUI: C1970107
Disease: ATAXIA, SPASTIC, 1, AUTOSOMAL DOMINANT
ATAXIA, SPASTIC, 1, AUTOSOMAL DOMINANT 		2 0 1 7.7E-02 0 0