Search Ontology:
Human Disease

hereditary spastic paraplegia 41

Term ID
DOID:0110793
Synonyms
  • autosomal dominant spastic paraplegia 41
  • autosomal dominant spastic paraplegia type 41
  • SPG41
Definition
A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 11p14.1-p11.2. https://www.ncbi.nlm.nih.gov/pubmed/18364116
References
Ontology
Human Disease   ( DOID:0110793 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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