hereditary spastic paraplegia 41

Term ID

DOID:0110793

Synonyms

• autosomal dominant spastic paraplegia 41
• autosomal dominant spastic paraplegia type 41
• SPG41

Definition

A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 11p14.1-p11.2. https://www.ncbi.nlm.nih.gov/pubmed/18364116

References

• ICD10CM:G11.4
• OMIM:613364
• ORDO:320355

Ontology

Human Disease   ( DOID:0110793 )