striatonigral degeneration

Summary
Disease Ontology
DOID:4751
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
23636 NUP62 nucleoporin 62
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
P37198 Nuclear pore glycoprotein p62
The Human Phenotype Ontology
Displaying entries 1 - 10 of 36 in total
HPO ID HPO Term
HP:0000648 Optic atrophy
HP:0000750 Delayed speech and language development
HP:0001251 Ataxia
HP:0001256 Intellectual disability, mild
HP:0001257 Spasticity
HP:0001260 Dysarthria
HP:0001266 Choreoathetosis
HP:0001276 Hypertonia
HP:0001285 Spastic tetraparesis
HP:0001288 Gait disturbance
Displaying 1 entry
Gene ID Gene Symbol Description
103 ADAR adenosine deaminase RNA specific

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: [email protected]

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.5.0

Last updated: April 6, 2026