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hereditary spastic paraplegia 11

Go to external page http://purl.obolibrary.org/obo/DOID_0110764

A hereditary spastic paraplegia that has_material_basis_in mutation in the SPG11 gene on chromosome 15q21. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

hereditary spastic paraplegia 11

Synonyms
  • HSP-TCC
  • Nakamura-Osame syndrome
  • SPG11
  • 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
  • spastic paraplegia-intellectual disability-thin corpus callosum syndrome
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disease_ontology

id

DOID:0110764