hereditary spastic paraplegia 45

Term ID

DOID:0110797

Synonyms

• autosomal recessive spastic paraplegia 45
• autosomal recessive spastic paraplegia type 45
• autosomal recessive spastic paraplegia type 65
• SPG45
• SPG65

Definition

A hereditary spastic paraplegia that has_material_basis_in mutation in the NT5C2 gene on chromosome 10q24. https://www.ncbi.nlm.nih.gov/pubmed/24482476

References

• ICD10CM:G11.4
• OMIM:613162
• ORDO:320396

Ontology

Human Disease   ( DOID:0110797 )