Certain specified rare distal myopathy (Q85565): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed label, description and/or aliases in pt-br, en |
Changed an Item |
||
| Property / Canonical URI | |||
| Property / Canonical URI: https://id.who.int/icd/entity/1760014100 / rank | |||
Normal rank | |||
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 |
||
| 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. |
