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Human Disease

hereditary spastic paraplegia 51

Term ID
DOID:0110803
Synonyms
  • autosomal dominant spastic paraplegia 51
  • CPSQ4
  • spastic quadriplegic cerebral palsy 4
  • SPG51
Definition
A hereditary spastic paraplegia that has_material_basis_in mutation in the AP4E1 gene on chromosome 15q21. (2)
References
Ontology
Human Disease   ( DOID:0110803 )
Relationships
is a type of
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Genes Involved
Zebrafish Models