OBO ID: DOID:0110812
Term Name: hereditary spastic paraplegia 61 Search Ontology:
Synonyms:
  • autosomal recessive spastic paraplegia 61
  • autosomal recessive spastic paraplegia type 61
  • SPG61
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the ARL6IP1 gene on chromosome 16p12. https://www.ncbi.nlm.nih.gov/pubmed/24482476
References:
Ontology: Human Disease   (DOID:0110812)
OTHER hereditary spastic paraplegia 61 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ARL6IP1 ?Spastic paraplegia 61, autosomal recessive 615685
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None