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Metadata
ID DOID:0110821
Name hereditary spastic paraplegia 76
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
Xrefs

OMIM:616907

Synonyms

autosomal recessive spastic paraplegia 76 [EXACT]

SPG76 [EXACT]

Parent Relationships

is_a hereditary spastic paraplegia

is_a autosomal recessive disease

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