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

OMIM:616907

Ontology

Human Disease ( DOID:0110821 )

Relationships

is a type of: autosomal recessive disease hereditary spastic paraplegia

autosomal recessive disease hereditary spastic paraplegia Show first 5 Terms

Other Pages

Alliance (1)

Genes Involved

Zebrafish Models

Citations