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Human Disease

hereditary spastic paraplegia 39

Term ID
DOID:0110790
Synonyms
  • autosomal recessive spastic paraplegia 39
  • autosomal recessive spastic paraplegia type 39
  • NTE-related motor neuron disorder
  • NTEMND
  • spastic paraplegia due to neuropathy target esterase mutation
  • spastic paraplegia due to NTE mutation
  • SPG39
Definition
A hereditary spastic paraplegia that has_material_basis_in mutation in the PNPLA6 gene on chromosome 19p13. https://www.ncbi.nlm.nih.gov/pubmed/18313024
References
Ontology
Human Disease   ( DOID:0110790 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models