Disease or Syndrome
congenital hemolytic anemia
Subclass of:
Genetic Diseases, Inborn; Anemia, Hemolytic
Definitions related to anemia, hemolytic, congenital:
  • (hereditary hemolytic anemia) A congenital hemolytic anemia caused by defects of the erythrocyte membrane, enzyme deficiencies, or hemoglobinopathies.
    NCI
    U.S. National Cancer Institute, 2021
  • (congenital hemolytic anemia) A form of hemolytic anemia with congenital onset.
    Human Phenotype Ontology (HPO)
    The Human Phenotype Ontology Project, 2025
  • (hereditary hemolytic anemia) Hemolytic anemia for which the cause is an inherited disorder.
    NICHD Pediatric Terminology
    U.S. National Cancer Institute, 2021
  • (congenital hemolytic anemia) Includes hereditary erythrocyte membrane defects, enzyme deficiencies, hemoglobin abnormalities, stem cell defects (paroxysmal nocturnal hemoglobinuria), and alloimmune (Rh) disease of newborn.
    CRISP Thesaurus
    National Institutes of Health, 2006
  • Hemolytic anemia due to various intrinsic defects of the erythrocyte.
    NLM Medical Subject Headings
    U.S. National Library of Medicine, 2025
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