Search Ontology:
Human Disease

hereditary spastic paraplegia 4

Term ID
DOID:0110792
Synonyms
  • autosomal dominant spastic paraplegia 4
  • autosomal dominant spastic paraplegia type 4
  • SPG4
Definition
A hereditary spastic paraplegia that is characterized by slowly progressive muscle weakness and spasticity and has_material_basis_in mutation in the SPAST gene on chromosome 2p22. https://www.ncbi.nlm.nih.gov/pubmed/9302257
References
Ontology
Human Disease   ( DOID:0110792 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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