OBO ID: DOID:0110808
Term Name: hereditary spastic paraplegia 56 Search Ontology:
Synonyms:
  • autosomal recessive spastic paraplegia 56
  • autosomal recessive spastic paraplegia type 56
  • SPG56
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the CYP2U1 gene on chromosome 4q25. https://www.ncbi.nlm.nih.gov/pubmed/23176821
References:
Ontology: Human Disease   (DOID:0110808)
OTHER hereditary spastic paraplegia 56 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CYP2U1 Spastic paraplegia 56, autosomal recessive 615030
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None