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Human Disease

hereditary spastic paraplegia 28

Term ID
DOID:0110779
Synonyms
  • autosomal recessive spastic paraplegia 28
  • autosomal recessive spastic paraplegia type 28
  • SPG28
Definition
A hereditary spastic paraplegia that has_material_basis_in mutation in the DDHD1 gene on chromosome 14q22. https://www.ncbi.nlm.nih.gov/pubmed/23176821
References
Ontology
Human Disease   ( DOID:0110779 )
Relationships
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Genes Involved
Zebrafish Models