Pyropoikilocytosis, hereditary
MONDO:0009948An autosomal recessive inherited severe hemolytic anemia. It is a subtype of hereditary elliptocytosis and is characterized by partial spectrin deficiency.
Also known as: Hypophosphatasia, pyropoikilocytosis, pyropoikilocytosis, hereditary, HPP, hereditary pyropoikilocytosis, pyropoikilocytosis hereditary
1 clinical trial for this condition and its sub-types.
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