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Disease Ontology Browser
Mast syndrome (DOID:0060245)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 21; autosomal recessive spastic paraplegia type 21; hereditary spastic paraplegia 21; SPG21
Alt IDs: OMIM:248900, ICD10CM:G11.4, MESH:C565409, ORDO:101001
Definition: A hereditary spastic paraplegia associated with dementia.


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
02/18/2020
MGI 6.14
The Jackson Laboratory