OBO ID: DOID:0110807
Term Name: hereditary spastic paraplegia 55 Search Ontology:
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)
OTHER hereditary spastic paraplegia 55 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
MTRFR Spastic paraplegia 55, autosomal recessive 615035
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None