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#620369 - CONGENITAL MYOPATHY 22B, SEVERE FETAL; CMYO22B
Cytogenetic locations: Epilepsy
Gene summaries Genetic tests Medical literature
#620351 - CONGENITAL MYOPATHY 22A, CLASSIC; CMYO22A
#614198 - MYASTHENIC SYNDROME, CONGENITAL, 16; CMS16
#613345 - HYPOKALEMIC PERIODIC PARALYSIS, TYPE 2; HOKPP2
#608390 - MYOTONIA, POTASSIUM-AGGRAVATED
LARYNGOSPASM, SEVERE NEONATAL EPISODIC, INCLUDED; SNEL, INCLUDED
Cytogenetic locations: 23822145
*603967 - SODIUM VOLTAGE-GATED CHANNEL, ALPHA SUBUNIT 4; SCN4A
Cytogenetic locations: 26700687
#170500 - HYPERKALEMIC PERIODIC PARALYSIS; HYPP
NORMOKALEMIC PERIODIC PARALYSIS, POTASSIUM-SENSITIVE, INCLUDED
Cytogenetic locations: 15555532
#170400 - HYPOKALEMIC PERIODIC PARALYSIS, TYPE 1; HOKPP1
Cytogenetic locations: 14504341
#168300 - PARAMYOTONIA CONGENITA; PMC
PARAMYOTONIA CONGENITA WITHOUT COLD PARALYSIS, INCLUDED
Cytogenetic locations: 14655280
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