Terminology Service for NFDI4Health
hereditary spastic paraplegia 76
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http://purl.obolibrary.org/obo/DOID_0110821
A hereditary spastic paraplegia that has_material_basis_in mutation in the CAPN1 gene on chromosome 11q13. [ http://purl.obolibrary.org/obo/ECO_0007645 ]
Term info
Label
hereditary spastic paraplegia 76
Synonyms
- SPG76
- autosomal recessive spastic paraplegia 76
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disease_ontology
id
DOID:0110821