Search Ontology:
Human Disease

hereditary spastic paraplegia 2

Term ID
DOID:0110773
Synonyms
  • spastic paraplegia type 2
  • SPG2
  • X-linked spastic paraplegia 2
Definition
A hereditary spastic paraplegia that has_material_basis_in mutation in the PLP1 gene on chromosome Xq22.2. https://www.ncbi.nlm.nih.gov/pubmed/8012387
References
Ontology
Human Disease   ( DOID:0110773 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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