MeSH Browser

MeSH Supplementary: Anemia, hereditary spherocytic hemolytic
Unique ID: C536356
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536356
Entry Term(s): Acholuric jaundice; Chronic acholuric jaundice; Congenital hemolytic jaundice; Debrie's familial haemolytic disease; Minkowski-Chauffard disease; Minkowski-Chauffard haemolytic jaundice; Minkowski-Chauffard-Gänsslen syndrome
Registry Numbers: 0
Heading Mapped to: *Spherocytosis, Hereditary; Ankyrins / deficiency; *Jaundice, Obstructive
Frequency: 91
Note: 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 of Entry: 2010/08/25
Revision Date: 2019/06/20

Anemia, hereditary spherocytic hemolytic MeSH Supplementary Concept Data 2025