Certain specified rare distal myopathy (Q85565): Difference between revisions
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Revision as of 10:55, 15 August 2026
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.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1760014100 |
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| English | Certain specified rare distal myopathy |
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. |
Statements
CID11:ID_1760014100
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