ORPHA:598

Multiminicore myopathy

Also called MmD, Multiminicore disease

Body system

Neurological diseases

Inheritance pattern

Autosomal dominant, Autosomal recessive

Typical age of onset

Antenatal, Childhood, Infancy, Neonatal

Estimated prevalence

Unknown (Worldwide)

Rarity class

Unknown

ORPHA:598 is classified under "Neurological diseases" in the Orphanet nomenclature.