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: C0558384
Disease: Arthritis/arthrosis
Arthritis/arthrosis 		1 0 1 7.7E-02 0 0
CUI: C0856123
Disease: Myotonia aggravated
Myotonia aggravated 		1 0 1 7.7E-02 0 0
CUI: C0858233
Disease: Stridor, Congenital
Stridor, Congenital 		1 0 1 7.7E-02 0 0
CUI: C1142081
Disease: Chronic lymphocytic leukaemia transformation
Chronic lymphocytic leukaemia transformation 		1 0 1 7.7E-02 0 0
CUI: C1853949
Disease: MYASTHENIA, FAMILIAL INFANTILE, 1
MYASTHENIA, FAMILIAL INFANTILE, 1 		1 0 1 7.7E-02 0 0
CUI: C1858891
Disease: PARAMYOTONIA CONGENITA/HYPERKALEMIC PERIODIC PARALYSIS
PARAMYOTONIA CONGENITA/HYPERKALEMIC PERIODIC PARALYSIS 		1 0 1 7.7E-02 0 0
CUI: C1868433
Disease: Normokalemic Periodic Paralysis, Potassium-Sensitive
Normokalemic Periodic Paralysis, Potassium-Sensitive 		1 0 1 7.7E-02 0 0
CUI: C1868619
Disease: Paramyotonia Congenita Without Cold Paralysis
Paramyotonia Congenita Without Cold Paralysis 		1 0 1 7.7E-02 0 0
CUI: C2931107
Disease: Myasthenic syndrome, congenital, postsynaptic slow-channel
Myasthenic syndrome, congenital, postsynaptic slow-channel 		1 0 1 7.7E-02 0 0
CUI: C3149517
Disease: LARYNGOSPASM, SEVERE NEONATAL EPISODIC
LARYNGOSPASM, SEVERE NEONATAL EPISODIC 		1 0 1 7.7E-02 0 0
CUI: C3280112
Disease: MYASTHENIC SYNDROME, CONGENITAL, 16
MYASTHENIC SYNDROME, CONGENITAL, 16 		1 0 1 7.7E-02 0 0
CUI: C3280402
Disease: SCLEROSTEOSIS 2
SCLEROSTEOSIS 2 		1 0 1 7.7E-02 0 0
CUI: C3489447
Disease: Hyperkalemic Periodic Paralysis Type 2
Hyperkalemic Periodic Paralysis Type 2 		1 0 1 7.7E-02 0 0
CUI: C3808739
Disease: MYASTHENIC SYNDROME, CONGENITAL, 8
MYASTHENIC SYNDROME, CONGENITAL, 8 		1 0 1 7.7E-02 0 0
CUI: C4016868
Disease: PARAMYOTONIA CONGENITA/MYOTONIA CONGENITA
PARAMYOTONIA CONGENITA/MYOTONIA CONGENITA 		1 0 1 7.7E-02 0 0
CUI: C4016869
Disease: MYOTONIA CONGENITA, ATYPICAL, ACETAZOLAMIDE-RESPONSIVE
MYOTONIA CONGENITA, ATYPICAL, ACETAZOLAMIDE-RESPONSIVE 		1 0 1 7.7E-02 0 0
CUI: C4022682
Disease: Cold-sensitive myotonia
Cold-sensitive myotonia 		1 0 1 7.7E-02 0 0
CUI: C4022684
Disease: Myotonia of the lower limb
Myotonia of the lower limb 		1 0 1 7.7E-02 0 0
CUI: C4022685
Disease: Myotonia of the jaw
Myotonia of the jaw 		1 0 1 7.7E-02 0 0
CUI: C4022686
Disease: Myotonia of the face
Myotonia of the face 		1 0 1 7.7E-02 0 0
CUI: C4022691
Disease: Facial muscle hypertrophy
Facial muscle hypertrophy 		1 0 1 7.7E-02 0 0
CUI: C4023179
Disease: Paradoxical myotonia
Paradoxical myotonia 		1 0 1 7.7E-02 0 0
CUI: C4225235
Disease: MYASTHENIC SYNDROME, CONGENITAL, 19
MYASTHENIC SYNDROME, CONGENITAL, 19 		1 0 1 7.7E-02 0 0
CUI: C4225367
Disease: MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY
MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY 		1 0 1 7.7E-02 0 0
CUI: C4225368
Disease: MYASTHENIC SYNDROME, CONGENITAL, 9, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY
MYASTHENIC SYNDROME, CONGENITAL, 9, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY 		1 0 1 7.7E-02 0 0