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Disease Ontology Browser
hereditary spastic paraplegia 62 (DOID:0110813)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 62; autosomal recessive spastic paraplegia type 62; SPG62
Alt IDs: OMIM:615681, ICD10CM:G11.4, ORDO:401785
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the ERLIN1 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
02/11/2020
MGI 6.14
The Jackson Laboratory