ORPHA:93613
Cystinuria type B
- Body system
- Inborn errors of metabolism
- Inheritance pattern
- Semi-dominant
- Typical age of onset
- Not documented in Orphadata
- Estimated prevalence
- Not documented in Orphadata
- Rarity class
- Not documented in Orphadata
ORPHA:93613 is classified under "Inborn errors of metabolism" in the Orphanet nomenclature.