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

• GARD:4919
• ICD10CM:G11.4
• MIM:604360
• ORDO:2822

Ontology

Human Disease   ( DOID:0110764 )