Strumpell-lorrain diseaseFamilial spastic paraplegiaSpastic ataxiaOther Metabolites Mapped to 'Hereditary spastic paraplegia'HMDB0000763 (5-Hydroxyindoleacetic acid) HMDB0001490 (Vanylglycol) HMDB0000929 (L-Tryptophan) HMDB0000118 (Homovanillic acid) HMDB0000235 (Thiamine)
- HMDB0000929 (L-Tryptophan)
- Hereditary spastic paraplegia
- 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.