Isolated glycerol kinase deficiency (Q98861): Difference between revisions

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+https://id.who.int/icd/entity/542432712
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+August 2026Timestamp +2026-08-15T00:00:00Z
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Calendar Gregorian
Precision 1 day
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@@ Property / Collection date: 15 August 2026 / rank @@
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Latest revision as of 15:30, 16 August 2026

This is an isolated X-linked recessive enzyme defect that is heterozygous in nature. Three clinically distinct forms of this deficiency have been proposed, namely infantile, juvenile, and adult.

Language	Label	Description	Also known as
default for all languages	ID_542432712
English	Isolated glycerol kinase deficiency	This is an isolated X-linked recessive enzyme defect that is heterozygous in nature. Three clinically distinct forms of this deficiency have been proposed, namely infantile, juvenile, and adult.