OBO ID: DOID:0110816
Term Name: hereditary spastic paraplegia 7 Search Ontology:
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)
OTHER hereditary spastic paraplegia 7 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SPG7 Spastic paraplegia 7, autosomal recessive 607259
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None