OBO ID: DOID:0110772
Term Name: hereditary spastic paraplegia 19 Search Ontology:
Synonyms:
  • autosomal dominant spastic paraplegia 19
  • autosomal dominant spastic paraplegia type 19
  • SPG19
Definition: A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 9q. https://www.ncbi.nlm.nih.gov/pubmed/12112072
References:
Ontology: Human Disease   ( DOID:0110772 )
OTHER hereditary spastic paraplegia 19 PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None