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Human Disease

hereditary spastic paraplegia 55

Term ID
DOID:0110807
Synonyms
  • autosomal recessive spastic paraplegia 55
  • autosomal recessive spastic paraplegia type 55
  • SPG55
Definition
A hereditary spastic paraplegia that has_material_basis_in mutation in the C12ORF65 gene on chromosome 12q24. https://www.ncbi.nlm.nih.gov/pubmed/23188110
References
Ontology
Human Disease   ( DOID:0110807 )
Relationships
is a type of
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Genes Involved
Zebrafish Models