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: C1828221
Disease: Non dystrophic myotonia
Non dystrophic myotonia 		3 0 2 0.29 0 0
CUI: C0019489
Disease: Deficiency, Hexosediphosphatase
Deficiency, Hexosediphosphatase 		1 0 1 0.17 0 0
CUI: C0410652
Disease: Cervical spine instability
Cervical spine instability 		1 0 1 0.17 0 0
CUI: C0685108
Disease: Lenegre's disease
Lenegre's disease 		1 0 1 0.17 0 0
CUI: C0748694
Disease: sick sinus
sick sinus 		1 0 1 0.17 0 0
CUI: C0856123
Disease: Myotonia aggravated
Myotonia aggravated 		1 0 1 0.17 0 0
CUI: C0856823
Disease: Undifferentiated type acute leukemia
Undifferentiated type acute leukemia 		1 0 1 0.17 0 0
CUI: C0862039
Disease: Precursor B-lymphoblastic lymphoma stage II
Precursor B-lymphoblastic lymphoma stage II 		1 0 1 0.17 0 0
CUI: C1336727
Disease: Testicular Sarcoma
Testicular Sarcoma 		1 0 1 0.17 0 0
CUI: C1832680
Disease: CARDIOMYOPATHY, DILATED, 1E
CARDIOMYOPATHY, DILATED, 1E 		1 0 1 0.17 0 0
CUI: C1838527
Disease: LONG QT SYNDROME 3, ACQUIRED, SUSCEPTIBILITY TO (finding)
LONG QT SYNDROME 3, ACQUIRED, SUSCEPTIBILITY TO (finding) 		1 0 1 0.17 0 0
CUI: C1858043
Disease: Hydronephrosis, Congenital, with Cleft Palate, Characteristic Facies, Hypotonia, and Mental Retardation
Hydronephrosis, Congenital, with Cleft Palate, Characteristic Facies, Hypotonia, and Mental Retardation 		1 0 1 0.17 0 0
CUI: C1858891
Disease: PARAMYOTONIA CONGENITA/HYPERKALEMIC PERIODIC PARALYSIS
PARAMYOTONIA CONGENITA/HYPERKALEMIC PERIODIC PARALYSIS 		1 0 1 0.17 0 0
CUI: C1861983
Disease: Heart Block, Nonprogressive
Heart Block, Nonprogressive 		1 0 1 0.17 0 0
CUI: C1861984
Disease: Cardiac Conduction Defect, Nonprogressive
Cardiac Conduction Defect, Nonprogressive 		1 0 1 0.17 0 0
CUI: C1864912
Disease: 2-Methylbutyryl-CoA Dehydrogenase Deficiency
2-Methylbutyryl-CoA Dehydrogenase Deficiency 		1 0 1 0.17 0 0
CUI: C1868433
Disease: Normokalemic Periodic Paralysis, Potassium-Sensitive
Normokalemic Periodic Paralysis, Potassium-Sensitive 		1 0 1 0.17 0 0
CUI: C1868619
Disease: Paramyotonia Congenita Without Cold Paralysis
Paramyotonia Congenita Without Cold Paralysis 		1 0 1 0.17 0 0
CUI: C2114320
Disease: preterm contractions
preterm contractions 		1 0 1 0.17 0 0
CUI: C2198591
Disease: 2-methylbutyrylglycinuria
2-methylbutyrylglycinuria 		1 0 1 0.17 0 0
CUI: C2216002
Disease: electrocardiogram left posterior hemiblock (finding)
electrocardiogram left posterior hemiblock (finding) 		1 0 1 0.17 0 0
CUI: C2930805
Disease: Sudden unexpected nocturnal death syndrome
Sudden unexpected nocturnal death syndrome 		1 0 1 0.17 0 0
CUI: C3149517
Disease: LARYNGOSPASM, SEVERE NEONATAL EPISODIC
LARYNGOSPASM, SEVERE NEONATAL EPISODIC 		1 0 1 0.17 0 0
CUI: C3151464
Disease: ATRIAL FIBRILLATION, FAMILIAL, 10
ATRIAL FIBRILLATION, FAMILIAL, 10 		1 0 1 0.17 0 0
CUI: C3280112
Disease: MYASTHENIC SYNDROME, CONGENITAL, 16
MYASTHENIC SYNDROME, CONGENITAL, 16 		1 0 1 0.17 0 0