Search Ontology:
Human Disease

hereditary spastic paraplegia 33

Term ID
DOID:0110784
Synonyms
  • autosomal dominant spastic paraplegia 33
  • SPG33
Definition
A hereditary spastic paraplegia that has_material_basis_in mutation in the ZFYVE27 gene on chromosome 10q24. https://www.ncbi.nlm.nih.gov/pubmed/16826525
References
Ontology
Human Disease   ( DOID:0110784 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models