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Adenosine triphosphatase deficiency, anemia due to

Orpha number ORPHA1044
Prevalence of rare diseases Unknown
Inheritance
  • Autosomal dominant
Age of onset No data available
ICD 10 code
  • E88.8
MIM number
Synonym(s) -

Summary

This syndrome is characterized by nonspherocytic hemolytic anemia due to deficiency of adenosine triphosphatase (ATPase). It has been described in two kindreds, in which at least two generations were affected. The syndrome is probably transmitted as a dominant trait. *Author: Orphanet (May 2006)*.

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