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Disease Ontology Browser
hereditary spastic paraplegia 81 (DOID:0112349)
Alliance: disease page
Synonyms: 'autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction'; 'autosomal recessive complex SPG due to Kennedy pathway dysfunction'; 'spastic paraplegia 81 autosomal recessive'; 'SPG81'
Alt IDs: OMIM:618768, ORDO:506353
Definition: A hereditary spastic paraplegia characterized by onset in infancy, delayed motor development, progressive spasticity, and other neurologic impairments that has_material_basis_in homozygous or compound heterozygous mutation in SELENOI on chromosome 2p23.3.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
06/23/2022
MGI 6.20
The Jackson Laboratory