OBO ID: DOID:0110764
Term Name: hereditary spastic paraplegia 11 Search Ontology:
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)
OTHER hereditary spastic paraplegia 11 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SPG11 Spastic paraplegia 11, autosomal recessive 604360
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS (1)