Search Ontology:
Human Disease

hereditary spastic paraplegia 27

Term ID
DOID:0110778
Synonyms
  • autosomal recessive spastic paraplegia 27
  • autosomal recessive spastic paraplegia type 27
  • SPG27
Definition
A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 10q22.1-q24.1. https://www.ncbi.nlm.nih.gov/pubmed/15455396
References
Ontology
Human Disease   ( DOID:0110778 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models