hereditary spastic paraplegia 55

Term ID

DOID:0110807

Synonyms

• autosomal recessive spastic paraplegia 55
• autosomal recessive spastic paraplegia type 55
• SPG55

Definition

A hereditary spastic paraplegia that has_material_basis_in mutation in the C12ORF65 gene on chromosome 12q24. https://www.ncbi.nlm.nih.gov/pubmed/23188110

References

• ICD10CM:G11.4
• OMIM:615035
• ORDO:320375

Ontology

Human Disease   ( DOID:0110807 )