Spherocytosis, Type 3 MeSH Supplementary Concept Data 2025

Details
Concepts

MeSH Supplementary: Spherocytosis, Type 3
Unique ID: C567489
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567489
Entry Term(s): Spherocytosis, Hereditary, 3
Registry Numbers: 0
Heading Mapped to: Spectrin / deficiency; *Spherocytosis, Hereditary
Frequency: 0
Note: aka SPH3 or HS3; mutations in SPTA1
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Spherocytosis, Type 3 Preferred

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