Search Ontology:
Human Disease

hereditary spastic paraplegia 25

Term ID
DOID:0110776
Synonyms
  • autosomal recessive spastic paraplegia 25
  • autosomal recessive spastic paraplegia type 25
  • SPG25
Definition
A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 6q23-q24.1. https://www.ncbi.nlm.nih.gov/pubmed/12070243
References
Ontology
Human Disease   ( DOID:0110776 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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