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hereditary spastic paraplegia 42
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http://purl.obolibrary.org/obo/DOID_0110794
A hereditary spastic paraplegia that has_material_basis_in mutation in the SLC33A1 gene on chromosome 3q25.31. [ http://purl.obolibrary.org/obo/ECO_0007645 ]
Term info
Label
hereditary spastic paraplegia 42
Synonyms
- SPG42
- autosomal dominant spastic paraplegia 42
- autosomal dominant spastic paraplegia type 42
has obo namespace
disease_ontology
id
DOID:0110794