OBO ID: DOID:0110814
Term Name: hereditary spastic paraplegia 63 Search Ontology:
Synonyms:
  • autosomal recessive spastic paraplegia 63
  • spastic paraplegia 63
  • SPG63
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the AMPD2 gene on chromosome 1p13. https://www.ncbi.nlm.nih.gov/pubmed/24482476
References:
Ontology: Human Disease   (DOID:0110814)
OTHER hereditary spastic paraplegia 63 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
AMPD2 ?Spastic paraplegia 63 615686
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None