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Human Disease

hereditary spastic paraplegia 29

Term ID
DOID:0110780
Synonyms
  • autosomal dominant spastic paraplegia 29
  • SPG29
Definition
A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 1p31.1-p21.1. https://www.ncbi.nlm.nih.gov/pubmed/16130112
References
Ontology
Human Disease   ( DOID:0110780 )
Relationships
is a type of
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Genes Involved
Zebrafish Models