Search Ontology:
Human Disease

hereditary spastic paraplegia 11

Term ID
DOID:0110764
Synonyms
  • autosomal recessive spastic paraplegia 11
  • autosomal recessive spastic paraplegia complicated with thin corpus callosum
  • autosomal recessive spastic paraplegia type 11
  • autosomal recessive spastic paraplegia with mental impairment and thin corpus callosum
  • HSP-TCC
  • Nakamura-Osame syndrome
  • spastic paraplegia-intellectual disability-thin corpus callosum syndrome
  • SPG11
Definition
A hereditary spastic paraplegia that has_material_basis_in mutation in the SPG11 gene on chromosome 15q21. https://www.ncbi.nlm.nih.gov/pubmed/17322883
References
Ontology
Human Disease   ( DOID:0110764 )
Relationships
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Genes Involved
Zebrafish Models