striatonigral degeneration

Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary

Literature (0)

DOID:4751 - striatonigral degeneration

Disease Ontology Definition:n_a

Synonyms:

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

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

: pde8b, nup62

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0003122 - pharyngeal arch artery 5

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

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, Ontobee

Parent(s): multiple system atrophy (is_a)