Information for "Medicine:Hemoglobin M disease"

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Display title	Medicine:Hemoglobin M disease
Default sort key	Hemoglobin M disease
Page length (in bytes)	24,671
Namespace ID	3048
Namespace	Medicine
Page ID	877305
Page content language	en - English
Page content model	wikitext
Indexing by robots	Allowed
Number of redirects to this page	0
Counted as a content page	Yes
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Page creator	imported>John Marlo
Date of page creation	21:25, 7 February 2024
Latest editor	imported>John Marlo
Date of latest edit	21:25, 7 February 2024
Total number of edits	1
Recent number of edits (within past 90 days)	0
Recent number of distinct authors	0

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Description	Content
Article description: (`description`) This attribute controls the content of the `description` and `og:description` elements.	Hemoglobin M disease is a rare form of hemoglobinopathy, characterized by the presence of hemoglobin M (HbM) and elevated methemoglobin (metHb) level in blood. HbM is an altered form of hemoglobin (Hb) due to point mutation occurring in globin-encoding genes, mostly involving tyrosine substitution for...

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