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Disease Ontology Browser
hereditary spastic paraplegia 9B (DOID:0110825)
Alliance: disease page
Synonyms: autosomal recessive complex spastic paraplegia type 9B; autosomal recessive spastic paraplegia 9B; SPG9B
Alt IDs: OMIM:616586, ICD10CM:G11.4, ORDO:447760
Definition: A hereditary spastic paraplegia that has_material_basis_in autosomal recessive homozygous or compound heterozygous mutation in the ALDH18A1 gene on chromosome 10q24.


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
01/24/2023
MGI 6.22
The Jackson Laboratory