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: 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: C1833508
Disease: CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET
CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET 		1 0 1 8.3E-02 0 0
CUI: C1833511
Disease: CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE
CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE 		1 0 1 8.3E-02 0 0
CUI: C1833518
Disease: CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL
CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL 		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: C1837273
Disease: Long-chain dicarboxylic aciduria
Long-chain dicarboxylic aciduria 		1 0 1 8.3E-02 0 0
CUI: C1881170
Disease: Inappropriate sinus tachycardia
Inappropriate sinus tachycardia 		1 0 1 8.3E-02 0 0
CUI: C3280160
Disease: ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 4
ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 4 		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: C4540171
Disease: 3-METHYLGLUTACONIC ACIDURIA, TYPE IX
3-METHYLGLUTACONIC ACIDURIA, TYPE IX 		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: C0750968
Disease: Central Nervous System Metabolic Disorders
Central Nervous System Metabolic Disorders 		2 0 1 7.7E-02 0 0
CUI: C0751743
Disease: Metabolic Disorder, Central Nervous System, Acquired
Metabolic Disorder, Central Nervous System, Acquired 		2 0 1 7.7E-02 0 0
CUI: C0751744
Disease: Brain Diseases, Metabolic, Acquired
Brain Diseases, Metabolic, Acquired 		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