OBO ID: DOID:0110784
Term Name: hereditary spastic paraplegia 33 Search Ontology:
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 )
OTHER hereditary spastic paraplegia 33 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ZFYVE27 Spastic paraplegia 33, autosomal dominant 610244
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None