Term Name: hereditary spastic paraplegia 7
Synonyms: autosomal recessive spastic paraplegia 7, spastic paraplegia type 7, SPG7
Definition: A hereditary spastic paraplegia that is characterized by slowly progressive onset, usually between 18-60 years of age, and generally more severe spasticity and has_material_basis_in mutation in the SPG7 gene on chromosome 16q24.
Ontology: Human Disease [DOID:0110816]   ( DOID:0110816 )

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