Anemia, hereditary spherocytic hemolytic [Supplementary Concept]

A rare hereditary form of spherocytosis caused by mutations in the ANKYRIN -1 gene (OMIM: 612641). Symptoms include jaundice, excessive fatigue, and delayed puberty.

Date introduced: August 25, 2010

MeSH Unique ID: C536356

Heading Mapped to:

• Spherocytosis, Hereditary
• Ankyrins/deficiency
• Jaundice, Obstructive

Entry Terms:

• Minkowski-Chauffard haemolytic jaundice
• Minkowski-Chauffard-Gänsslen syndrome
• Acholuric jaundice
• Congenital hemolytic jaundice
• Chronic acholuric jaundice
• Minkowski-Chauffard disease
• Debrie's familial haemolytic disease