Hemoglobinopathies/Definition: Difference between revisions

From Citizendium
Jump to navigation Jump to search
imported>Howard C. Berkowitz
(New page: <noinclude>{{Subpages}}</noinclude> A group of inherited disorders characterized by structural alterations within the hemoglobin molecule (National Library of Medicine; the plural ...)
 
imported>Daniel Mietchen
(.<noinclude>{{DefMeSH}}</noinclude>)
 
Line 1: Line 1:
<noinclude>{{Subpages}}</noinclude>
<noinclude>{{Subpages}}</noinclude>
A group of inherited disorders characterized by structural alterations within the [[hemoglobin]] molecule ([[National Library of Medicine]]; the plural is the MeSH indexing term)
A group of inherited disorders characterized by structural alterations within the [[hemoglobin]] molecule.<noinclude>{{DefMeSH}}</noinclude>

Latest revision as of 18:04, 14 May 2010

This article contains just a definition and optionally other subpages (such as a list of related articles), but no metadata. Create the metadata page if you want to expand this into a full article.


Hemoglobinopathies [r]: A group of inherited disorders characterized by structural alterations within the hemoglobin molecule.

This definition is at least in part based on: Anonymous (2024), Hemoglobinopathies (English). Medical Subject Headings. U.S. National Library of Medicine.