OBO ID: DOID:0110766
Term Name: hereditary spastic paraplegia 13 Search Ontology:
Synonyms:
  • autosomal dominant spastic paraplegia 13
  • SPG13
Definition: A hereditary spastic paraplegia that is characterized by a pure form of the disease with late onset and has_material_basis_in mutation in the HSPD1 on chromosome 2q33. https://www.ncbi.nlm.nih.gov/pubmed/11898127
References:
Ontology: Human Disease   (DOID:0110766)
OTHER hereditary spastic paraplegia 13 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
HSPD1 Spastic paraplegia 13, autosomal dominant 605280
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None