Terminology Service for NFDI4Health
hereditary spastic paraplegia 10
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http://purl.obolibrary.org/obo/DOID_0110763
A hereditary spastic paraplegia that has_material_basis_in mutation in the KIF5A gene on chromosome 12q13. [ http://purl.obolibrary.org/obo/ECO_0007645 ]
Term info
Label
hereditary spastic paraplegia 10
Synonyms
- SPG10
- autosomal dominant spastic paraplegia 10
- autosomal dominant spastic paraplegia type 10
has obo namespace
disease_ontology
id
DOID:0110763