hereditary spherocytic hemolytic Anemia
A rare hereditary form of spherocytosis caused by mutations in the ANKYRIN -1 gene (OMIM: 612641). Symptoms include jaundice, excessive fatigue, and delayed puberty.
Also Known As:
Anemia, hereditary spherocytic hemolytic; Acholuric jaundice; Chronic acholuric jaundice; Congenital hemolytic jaundice; Debrie's familial haemolytic disease; Minkowski-Chauffard disease; Minkowski-Chauffard haemolytic jaundice; Minkowski-Chauffard-Gänsslen syndrome
Networked: 29
relevant articles (1 outcomes,
2 trials/studies)
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Disease Context: Research Results
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Drugs and Important Biological Agents (IBA) related to hereditary spherocytic hemolytic Anemia:
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