hereditary spastic paraplegia 27

Term ID

DOID:0110778

Synonyms

• autosomal recessive spastic paraplegia 27
• autosomal recessive spastic paraplegia type 27
• SPG27

Definition

A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 10q22.1-q24.1. https://www.ncbi.nlm.nih.gov/pubmed/15455396

References

• ICD10CM:G11.4
• OMIM:609041
• ORDO:101007

Ontology

Human Disease   ( DOID:0110778 )