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Disease Ontology Browser
hereditary spastic paraplegia 92 (DOID:0070644)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 92; SPG92
Alt IDs: OMIM:620911
Definition: A hereditary spastic paraplegia that has_material_basis_in homozygous or compound heterozygous mutation in the FICD gene on chromosome 12q23.


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
03/18/2025
MGI 6.24
The Jackson Laboratory