Search Ontology:
Human Disease

hereditary spastic paraplegia 19

Term ID
DOID:0110772
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 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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