Search Ontology:
Human Disease

hereditary spastic paraplegia 63

Term ID
DOID:0110814
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 )
Relationships
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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