Spastic Paraplegia 35

**Semantic type:** Disease or Syndrome

**Definition:** An autosomal recessive subtype of hereditary spastic paraplegia caused by mutation(s) in the FA2H gene, encoding fatty acid 2-hydroxylase.

**Synonyms:** - FAHN - Fatty Acid Hydroxylase-Associated Neurodegeneration - SPG35 - Spastic Paraplegia 35, Autosomal Recessive, with or without Neurodegeneration