hereditary spastic paraplegia 33

Term ID

DOID:0110784

Synonyms

• autosomal dominant spastic paraplegia 33
• SPG33

Definition

A hereditary spastic paraplegia that has_material_basis_in mutation in the ZFYVE27 gene on chromosome 10q24. https://www.ncbi.nlm.nih.gov/pubmed/16826525

References

• OMIM:610244

Ontology

Human Disease   ( DOID:0110784 )