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Human Disease

hereditary spastic paraplegia 53

Term ID
DOID:0110805
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 )
Relationships
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Genes Involved
Zebrafish Models