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Disease Ontology Browser
hereditary spastic paraplegia 33 (DOID:0110784)
Alliance: disease page
Synonyms: autosomal dominant spastic paraplegia 33; SPG33
Alt IDs: OMIM:610244
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the ZFYVE27 gene on chromosome 10q24.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
12/05/2017
MGI 6.11
The Jackson Laboratory