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Disease Ontology Browser
hereditary spastic paraplegia 93 (DOID:0070645)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 93
Alt IDs: OMIM:620938
Definition: A hereditary spastic paraplegia that has_material_basis_in homozygous or compound heterozygous mutation in the NFU1 gene on chromosome 2p13.

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
07/29/2025
MGI 6.24 		The Jackson Laboratory