OBO ID: DOID:0110786
Term Name: hereditary spastic paraplegia 35 Search Ontology:
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)
OTHER hereditary spastic paraplegia 35 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
FA2H Spastic paraplegia 35, autosomal recessive 612319
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None