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Disease Ontology Browser
hereditary spastic paraplegia 89 (DOID:0070458)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 89; SPG89
Alt IDs: OMIM:620379
Definition: A hereditary spastic paraplegia characterized by infantile or early childhood onset of lower limb spasticity that has_material_basis_in homozygous mutation in the AMFR gene on chromosome 16q13.

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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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory