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Disease Ontology Browser
hereditary spastic paraplegia 18 (DOID:0110771)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 18; autosomal recessive spastic paraplegia type 18; IDMDC; intellectual disability, motor dysfunction and joint contractures; SPG18
Alt IDs: OMIM:611225, ICD10CM:G11.4, ORDO:209951
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the ERLIN2 gene on chromosome 8p11.


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
01/31/2023
MGI 6.22
The Jackson Laboratory