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hereditary spastic paraplegia 3A

http://purl.obolibrary.org/obo/DOID_0110791

A hereditary spastic paraplegia that is characterized by lower limb weakness and spasticity that is generally non-progressive or extremely slow and has_material_basis_in mutation in the ATL1 gene on chromosome 14q22. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

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Term info

Label

hereditary spastic paraplegia 3A

Synonyms

FSP1
SPG3A
autosomal dominant familial spastic paraplegia 1
autosomal dominant spastic paraplegia 3
autosomal dominant spastic paraplegia type 3
strumpell disease

database cross reference

has obo namespace

disease_ontology

DOID:0110791

Term relations

Subclass of:

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