ORPHA:612
Potassium-aggravated myotonia
Also called K+-aggravated myotonia, K-aggravated myotonia, PAM
- Body system
- Neurological diseases
- Inheritance pattern
- Autosomal dominant
- Typical age of onset
- Childhood
- Estimated prevalence
- Unknown (Worldwide)
- Rarity class
- Unknown
ORPHA:612 is classified under "Neurological diseases" in the Orphanet nomenclature.