striatonigral degeneration

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:4751 - striatonigral degeneration

Disease Ontology Definition:n_a

Synonyms:

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

OMIM:

MIM:271930 - striatonigral degeneration, infantile; sndi
MIM:609161 - striatal degeneration, autosomal dominant; adsd

MIM:271930 - striatonigral degeneration, infantile; sndi

MIM:609161 - striatal degeneration, autosomal dominant; adsd

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): multiple system atrophy (is_a)