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Hyperprolinaemia, type II

Orpha number ORPHA79101
Prevalence of rare diseases Unknown
Inheritance
  • Autosomal recessive
Age of onset Variable
ICD 10 code -
MIM number
Synonym(s) Delta1-pyrroline-5-carboxylate dehydrogenase deficiency

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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