ORPHA:284411
Glycerol kinase deficiency, juvenile form
- Body system
- Inborn errors of metabolism
- Inheritance pattern
- X-linked recessive
- Typical age of onset
- Adolescent, Childhood
- Estimated prevalence
- Not documented in Orphadata
- Rarity class
- Not documented in Orphadata
ORPHA:284411 is classified under "Inborn errors of metabolism" in the Orphanet nomenclature.