OBO ID: DOID:0110815
Term Name: hereditary spastic paraplegia 64 Search Ontology:
Synonyms:
  • autosomal recessive spastic paraplegia 64
  • autosomal recessive spastic paraplegia type 64
  • SPG64
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the ENTPD1 gene on chromosome 10q24. https://www.ncbi.nlm.nih.gov/pubmed/24482476
References:
Ontology: Human Disease   (DOID:0110815)
OTHER hereditary spastic paraplegia 64 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ENTPD1 Spastic paraplegia 64, autosomal recessive 615683
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None