OBO ID: DOID:0110788
Term Name: hereditary spastic paraplegia 37 Search Ontology:
Synonyms:
  • autosomal dominant spastic paraplegia 37
  • autosomal dominant spastic paraplegia type 37
  • SPG37
Definition: A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 8p21.1-q13.3. https://www.ncbi.nlm.nih.gov/pubmed/17605047
References:
Ontology: Human Disease   ( DOID:0110788 )
OTHER hereditary spastic paraplegia 37 PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None