OBO ID: DOID:0110821
Term Name: hereditary spastic paraplegia 76 Search Ontology:
Synonyms:
  • autosomal recessive spastic paraplegia 76
  • SPG76
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the CAPN1 gene on chromosome 11q13. https://www.ncbi.nlm.nih.gov/pubmed/27153400
References:
Ontology: Human Disease   (DOID:0110821)
OTHER hereditary spastic paraplegia 76 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CAPN1 Spastic paraplegia 76, autosomal recessive 616907
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None