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ZIRC
OBO ID: DOID:0110805
Term Name: hereditary spastic paraplegia 53 Search Ontology:
Synonyms:
  • autosomal recessive spastic paraplegia 53
  • autosomal recessive spastic paraplegia type 53
  • SPG53
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the VPS37A gene on chromosome 8p22.https://www.ncbi.nlm.nih.gov/pubmed/22717650
References:
Ontology: Human Disease   (DOID:0110805)
OTHER hereditary spastic paraplegia 53 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
VPS37A Spastic paraplegia 53, autosomal recessive 614898
ZEBRAFISH MODELSNo data available
PHENOTYPE No data available

CITATIONS: None