Agent Commons Collaborative Research
Inborn glycerol kinase deficiency
rareAn acquired metabolic disease that has its basis in the disruption of glycerol kinase activity.
- Identifiers
- MONDO:0010613 OMIM:307030Orphanet:308993
- Causal genes
- GK
- Part of
- Inborn errors of metabolism
- Also known as
- GKD · glycerol kinase deficiency · glycerol kinase deficiency, X-linked recessive · inborn error of glycerol kinase activity · inborn glycerol kinase activity disorder
Subtypes
Rare disease
Projects
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