Catalog

Certain specified rare distal myopathy

No MMS code

Link to WHO Definition

Certain specified rare distal myopathy – http://id.who.int/icd/entity/1760014100

Rare progressive genetic disorders characterised by wasting and weakness of the voluntary muscles of the distal extremities of upper and lower limbs. Although age of onset can occur anytime from infancy to adulthood, most forms develop later in life and are slowly progressive. Inheritance is autosomal dominant or recessive.