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hereditary spastic paraplegia 4

http://purl.obolibrary.org/obo/DOID_0110792

A hereditary spastic paraplegia that is characterized by slowly progressive muscle weakness and spasticity and has_material_basis_in mutation in the SPAST gene on chromosome 2p22. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

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Term info

Label

hereditary spastic paraplegia 4

Synonyms

SPG4
autosomal dominant spastic paraplegia 4
autosomal dominant spastic paraplegia type 4

database cross reference

has obo namespace

disease_ontology

DOID:0110792

Term relations

Subclass of:

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