Sarcoglycanopathies

**Definition:** Deficiencies or mutations in the genes for the SARCOGLYCAN COMPLEX subunits. A variety of phenotypes are associated with these mutations including a subgroup of autosomal recessive limb girdle muscular dystrophies, cardiomyopathies, and respiratory deficiency.

**Tree numbers:** - C05.651.534.500.280.500 - C08.618.923 - C10.668.491.175.500.149.500 - C14.280.238.812 - C16.320.577.280.500

**Synonyms:** - Sarcoglycanopathy