Search Ontology:
Human Disease

hereditary spastic paraplegia 42

Term ID
DOID:0110794
Synonyms
  • autosomal dominant spastic paraplegia 42
  • autosomal dominant spastic paraplegia type 42
  • SPG42
Definition
A hereditary spastic paraplegia that has_material_basis_in mutation in the SLC33A1 gene on chromosome 3q25.31. https://www.ncbi.nlm.nih.gov/pubmed/19061983
References
Ontology
Human Disease   ( DOID:0110794 )
Relationships
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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