hereditary spastic paraplegia 25

Term ID

DOID:0110776

Synonyms

• autosomal recessive spastic paraplegia 25
• autosomal recessive spastic paraplegia type 25
• SPG25

Definition

A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 6q23-q24.1. https://www.ncbi.nlm.nih.gov/pubmed/12070243

References

• GARD:9582
• ICD10CM:G11.4
• OMIM:608220
• ORDO:101005

Ontology

Human Disease   ( DOID:0110776 )