Terminology Service for NFDI4Health

hereditary spastic paraplegia 35

Go to external page http://purl.obolibrary.org/obo/DOID_0110786


A hereditary spastic paraplegia that has_material_basis_in mutation in the FA2H gene on chromosome 16q23.1. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

hereditary spastic paraplegia 35

Synonyms
  • FAHN
  • SPG35
  • autosomal recessive spastic paraplegia 35
  • autosomal recessive spastic paraplegia type 35
  • fatty acid hydroxylase-associated neurodegeneration
  • leukodystrophy, dysmyelinating and spastic paraparesis with or without dystonia
database cross reference
has obo namespace

disease_ontology

id

DOID:0110786