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DOID:0060245 - Mast syndrome
Disease Ontology Definition:A hereditary spastic paraplegia associated with dementia.
Synonyms: SPG21, autosomal recessive spastic paraplegia 21, autosomal recessive spastic paraplegia type 21, hereditary spastic paraplegia 21,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0009568 - mast syndrome |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
hereditary spastic paraplegia (is_a)