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hereditary spastic paraplegia 13

http://purl.obolibrary.org/obo/DOID_0110766

A hereditary spastic paraplegia that is characterized by a pure form of the disease with late onset and has_material_basis_in mutation in the HSPD1 on chromosome 2q33. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

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Term info

Label

hereditary spastic paraplegia 13

Synonyms

SPG13
autosomal dominant spastic paraplegia 13

database cross reference

has obo namespace

disease_ontology

DOID:0110766

Term relations

Subclass of:

autosomal dominant disease
hereditary spastic paraplegia
has material basis in some autosomal dominant inheritance