Neuroacanthocytosis, Mcleod Type MeSH Supplementary Concept Data 2025

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Concepts

MeSH Supplementary: Neuroacanthocytosis, Mcleod Type
Unique ID: C564038
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564038
Entry Term(s): McLeod Syndrome
Registry Numbers: 0
Heading Mapped to: *Neuroacanthocytosis
Frequency: 42
Note: mutation in XK gene
Date of Entry: 2012/11/05
Revision Date: 2013/10/24

Neuroacanthocytosis, Mcleod Type Preferred

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