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Summary Literature (0)
DOID:4751 - striatonigral degeneration

Disease Ontology Definition:n_a

Synonyms:

Xenbase Genes : pde8b, nup62

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0003122 - pharyngeal arch artery 5

MIM:
MIM:271930 - STRIATONIGRAL DEGENERATION, INFANTILE; SNDI
MIM:500003 - STRIATONIGRAL DEGENERATION, INFANTILE, MITOCHONDRIAL
MIM:609161 - STRIATAL DEGENERATION, AUTOSOMAL DOMINANT 1; ADSD1

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view
Parent(s): multiple system atrophy (is_a)