OBO ID: DOID:0110820
Term Name: hereditary spastic paraplegia 75 Search Ontology:
Synonyms:
  • autosomal recessive spastic paraplegia 75
  • autosomal recessive spastic paraplegia type 75
  • SPG75
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the MAG gene on chromosome 19q13. https://www.ncbi.nlm.nih.gov/pubmed/24482476
References:
Ontology: Human Disease   (DOID:0110820)
OTHER hereditary spastic paraplegia 75 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
MAG Spastic paraplegia 75, autosomal recessive 616680
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None