OBO ID: DOID:0110782
Term Name: hereditary spastic paraplegia 31 Search Ontology:
Synonyms:
  • autosomal dominant spastic paraplegia 31
  • autosomal dominant spastic paraplegia type 31
  • SPG31
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the REEP1 gene on chromosome 2p11. https://www.ncbi.nlm.nih.gov/pubmed/16826527
References:
Ontology: Human Disease   (DOID:0110782)
OTHER hereditary spastic paraplegia 31 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
REEP1 Spastic paraplegia 31, autosomal dominant 610250
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None