Inborn glycerol kinase deficiency

MONDO:0010613

An acquired metabolic disease that has its basis in the disruption of glycerol kinase activity.

Also known as: glycerol kinase deficiency, glycerol kinase deficiency, X-linked recessive, inborn error of glycerol kinase activity, inborn glycerol kinase activity disorder, rare inborn error of glycerol kinase activity, GK deficiency, GK1 deficiency, GKD

0 clinical trials for this condition and its sub-types, 0 tagged with Inborn glycerol kinase deficiency itself.

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Part of

↑ Inborn errors of metabolism (2228)

Sub-types of Inborn glycerol kinase deficiency

Chromosome Xp21 deletion syndrome 0 trials
Glycerol kinase deficiency, infantile form 0 trials
Isolated glycerol kinase deficiency 0 trials
2 sub-types
- Glycerol kinase deficiency, adult form 0 trials
- Glycerol kinase deficiency, juvenile form 0 trials

Including sub-types (0) Tagged with Inborn glycerol kinase deficiency (0)

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