OBO ID: DOID:0110817
Term Name: hereditary spastic paraplegia 72 Search Ontology:
Synonyms:
  • autosomal spastic paraplegia type 72
  • SPG72
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the REEP2 gene on chromosome 5q31. https://www.ncbi.nlm.nih.gov/pubmed/24388663
References:
Ontology: Human Disease   (DOID:0110817)
OTHER hereditary spastic paraplegia 72 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
REEP2 ?Spastic paraplegia 72, autosomal recessive 615625
?Spastic paraplegia 72, autosomal dominant 615625
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None