8C70.41 Recessive limb-girdle muscular dystrophy

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01


Autosomal recessive limb girdle muscular dystrophies (LGMD2) are a group of genetically heterogeneous diseases that are typically characterised by progressive weakness and wasting of the shoulder and pelvic girdle muscles. Many of the more than 20 different conditions show overlapping clinical features with other forms of muscular dystrophy, congenital, myofibrillar or even distal myopathies and also with acquired muscle diseases. Although individually extremely rare, all types of LGMD2 together form an important differential diagnostic group among neuromuscular diseases.

exclusions

postcoordination

Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.

Laterality  - only one may be selected
Specific anatomy  - multiple selections are allowed

synonyms

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