Term Name: hereditary spastic paraplegia 28
Synonyms: autosomal recessive spastic paraplegia 28, autosomal recessive spastic paraplegia type 28, SPG28
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the DDHD1 gene on chromosome 14q22.
Ontology: Human Disease [DOID:0110779]   ( DOID:0110779 )

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