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hereditary spastic paraplegia 6

Go to external page http://purl.obolibrary.org/obo/DOID_0110811

A hereditary spastic paraplegia that is usually characterized by rapidly progressive and severe spastic paraplegia and has_material_basis_in mutation in the NIPA1 gene on chromosome 15q11.2. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

hereditary spastic paraplegia 6

Synonyms
  • FSP3
  • SPG6
  • autosomal dominant familial spastic paraplegia type 3
  • autosomal dominant spastic paraplegia 6
  • autosomal dominant spastic paraplegia type 6
database cross reference
has obo namespace

disease_ontology

id

DOID:0110811