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Human Disease

hereditary spastic paraplegia 31

Term ID
DOID:0110782
Synonyms
  • autosomal dominant spastic paraplegia 31
  • autosomal dominant spastic paraplegia type 31
  • SPG31
Definition
A hereditary spastic paraplegia that has_material_basis_in mutation in the REEP1 gene on chromosome 2p11. https://www.ncbi.nlm.nih.gov/pubmed/16826527
References
Ontology
Human Disease   ( DOID:0110782 )
Relationships
is a type of
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Genes Involved
Zebrafish Models