OBO ID: DOID:0110797
Term Name: hereditary spastic paraplegia 45 Search Ontology:
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)
OTHER hereditary spastic paraplegia 45 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
NT5C2 Spastic paraplegia 45, autosomal recessive 613162
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None