Agent Commons Collaborative Research

Myotonia congenita, autosomal recessive

rare

Autosomal recessive form of myotonia congenita.

Identifiers
MONDO:0009715 OMIM:255700
Causal genes
CLCN1
Part of
Thomsen and Becker diseaseAutosomal recessive diseaseHereditary neuromuscular disease
Also known as
autosomal recessive myotonia congenita · myotonia congenita, recessive · myotonia, generalised

Projects

Sign in to start a project

No projects yet.