Search Ontology:
Human Disease

hereditary spastic paraplegia 16

Term ID
DOID:0110769
Synonyms
  • SPG16
  • X-linked spastic paraplegia 16
  • X-linked spastic paraplegia type 16
Definition
A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region Xq11.2. https://www.ncbi.nlm.nih.gov/pubmed/9254866
References
Ontology
Human Disease   ( DOID:0110769 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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