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Human Disease

hereditary spastic paraplegia 45

Term ID
DOID:0110797
Synonyms
  • autosomal recessive spastic paraplegia 45
  • autosomal recessive spastic paraplegia type 45
  • autosomal recessive spastic paraplegia type 65
  • SPG45
  • SPG65
Definition
A hereditary spastic paraplegia that has_material_basis_in mutation in the NT5C2 gene on chromosome 10q24. https://www.ncbi.nlm.nih.gov/pubmed/24482476
References
Ontology
Human Disease   ( DOID:0110797 )
Relationships
is a type of
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Genes Involved
Zebrafish Models