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Pyropoikilocytosis, hereditary

MONDO:0009948

An 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, 1 tagged with Pyropoikilocytosis, hereditary itself.

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Including sub-types (1) Tagged with Pyropoikilocytosis, hereditary (1)

Trials to join now! 1

New study aims to personalize care for rare blood disorders

Knowledge-focused Recruiting now

This study is for people with sickle cell disease or other rare anemias. Researchers want to use advanced genetic and blood tests to better understand each person's condition. The goal is to make diagnosis more precise so that treatments can be tailored to each patient. About 200…

Sponsor: Hospital Universitari Vall d'Hebron Research Institute • Aim: Knowledge-focused

Last updated Jun 27, 2026 07:53 UTC

Pyropoikilocytosis, hereditary

Where it sits in the disease tree

New study aims to personalize care for rare blood disorders