hereditary spastic paraplegia 33
MONDO:0012448Mondo
Findings
No curated finding names hereditary spastic paraplegia 33 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the ZFYVE27 gene.
Definition from the Mondo Disease Ontology (MONDO:0012448), read 2026-09-29. CC BY 4.0.
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- ZFYVE27HGNC:26559
- Limited · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2017
- Limited · PanelApp Australia · Autosomal dominant · 2025
- Disputed Evidence · ClinGen · Autosomal dominant · 2023
Where it sits
- A kind of
Other names
4 names
Resolves to: hereditary spastic paraplegia 33
- Also called
- hereditary spastic paraplegia caused by mutation in ZFYVE27hereditary spastic paraplegia type 33SPG33ZFYVE27 hereditary spastic paraplegia