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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.

Disease References using Mouse Models (1)
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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Send questions and comments to User Support. 		last database update
10/29/2024
MGI 6.24 		The Jackson Laboratory