Search Ontology:
Human Disease

hereditary spastic paraplegia 38

Term ID
DOID:0110789
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 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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