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Congenital muscular dystrophy with integrin deficiency

Orpha number ORPHA34520
Prevalence of rare diseases <1 / 1 000 000
Inheritance
  • Autosomal recessive
Age of onset Neonatal/infancy
ICD 10 code -
MIM number -
Synonym(s) -

Summary


An Orphanet summary for this disease is currently under development. However, other data related to the disease are accessible from the Additional Information menu located on the right side of this page.




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