Search Ontology:
Human Disease

hereditary spastic paraplegia 7

Term ID
DOID:0110816
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. https://www.ncbi.nlm.nih.gov/pubmed/9635427
References
Ontology
Human Disease   ( DOID:0110816 )
Relationships
is a type of
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Genes Involved
Zebrafish Models