Bethlem myopathy
MONDO:0008029A usually autosomal dominant inherited movement disorder caused by mutations in the COL6A1, COL6A2, and COL6A3 genes. It is characterized by progressive muscle weakness and joint stiffness in the fingers, wrists, elbows, and ankles.
Also known as: Bethlem myopathy type 1, benign autosomal dominant myopathy, BTHLM1, Bethlem myopathy 1
6 clinical trials for this condition and its sub-types, 0 tagged with Bethlem myopathy itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Part of
Sub-types of Bethlem myopathy
-
Bethlem myopathy 1A 0 trials
-
Bethlem myopathy 1B 0 trials
-
Bethlem myopathy 1C 0 trials
-
Bethlem myopathy 2 0 trials
We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.