- Compound
- CDB004871 (L-Tryptophan)
- Term
- Hereditary spastic paraplegia
- Definition
- A paraplegia that is characterized by progressive stiffness and contraction (spasticity) in the lower limbs. (do).
- Parent Term
- Health condition
- Parent Definition
- A health effect that consists on short or long-term disease, condition, disorder, syndrome or constant abnormality.
- Synonyms
Strumpell-lorrain diseaseFamilial spastic paraplegiaSpastic ataxiaOther Compounds Mapped to 'Hereditary spastic paraplegia'CDB004871 (L-Tryptophan)References