Search Ontology:
Human Disease

hereditary spastic paraplegia 37

Term ID
DOID:0110788
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 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models