Search Ontology:
Human Disease

hereditary spastic paraplegia 35

Term ID
DOID:0110786
Synonyms
  • autosomal recessive spastic paraplegia 35
  • autosomal recessive spastic paraplegia type 35
  • FAHN
  • fatty acid hydroxylase-associated neurodegeneration
  • leukodystrophy, dysmyelinating and spastic paraparesis with or without dystonia
  • SPG35
Definition
A hereditary spastic paraplegia that has_material_basis_in mutation in the FA2H gene on chromosome 16q23.1. https://www.ncbi.nlm.nih.gov/pubmed/19068277
References
Ontology
Human Disease   ( DOID:0110786 )
Relationships
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Genes Involved
Zebrafish Models