Term Name: hereditary spastic paraplegia 33
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.
Ontology: Human Disease [DOID:0110784]   ( DOID:0110784 )

Relationships
is a type of: autosomal dominant disease hereditary spastic paraplegia