Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Echinobase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Echinobase
Summary Literature (0)
DOID:0060245 - Mast syndrome

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

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

Echinobase Genes : spg21


MIM:
MIM:248900 - 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)