hereditary spastic paraplegia 31

Term ID

DOID:0110782

Synonyms

• autosomal dominant spastic paraplegia 31
• autosomal dominant spastic paraplegia type 31
• SPG31

Definition

A hereditary spastic paraplegia that has_material_basis_in mutation in the REEP1 gene on chromosome 2p11. https://www.ncbi.nlm.nih.gov/pubmed/16826527

References

• GARD:10817
• ICD10CM:G11.4
• OMIM:610250
• ORDO:101011

Ontology

Human Disease   ( DOID:0110782 )