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Human Disease

hereditary spastic paraplegia 76

Term ID
DOID:0110821
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 )
Relationships
is a type of
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Genes Involved
Zebrafish Models