1. Diseases
  2. Thomsen and Becker disease

Thomsen and Becker disease

Disease Export to PDF
Name:
Thomsen and Becker disease
Description:
A rare, genetic, skeletal muscle channelopathy characterized by slow muscle relaxation after contraction (myotonia).
ORPHAcode:
614
Synonyms:
Myotonia congenita
XREF(s):
Orphanet
MedDRA
MedDRA
ICD-10
OMIM
OMIM
Analyte(s):
CLCN1
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14