Search Ontology:
Human Disease
hereditary spastic paraplegia 33
- Term ID
- DOID:0110784
- Synonyms
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- 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
- Ontology
- Human Disease ( DOID:0110784 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models