OBO ID: DOID:0110789
Term Name: hereditary spastic paraplegia 38 Search Ontology:
Synonyms:
  • autosomal dominant spastic paraplegia 38
  • autosomal dominant spastic paraplegia type 38
  • SPG38
Definition: A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 4p16-p15. https://www.ncbi.nlm.nih.gov/pubmed/18401025
References:
Ontology: Human Disease   ( DOID:0110789 )
OTHER hereditary spastic paraplegia 38 PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None