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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, ORDO:101001
Definition: A hereditary spastic paraplegia associated with dementia.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.12
The Jackson Laboratory