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Summary Literature (0)
DOID:0060245 - Mast syndrome

Disease Ontology Definition:A hereditary spastic paraplegia associated with dementia.

Synonyms: autosomal recessive spastic paraplegia 21, autosomal recessive spastic paraplegia type 21, hereditary spastic paraplegia 21, SPG21

Xenbase Genes : spg21

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009568 - mast syndrome


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): hereditary spastic paraplegia (is_a)