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Standards Ontologies Notations
striatonigral degeneration

Summary
Super Class
multiple system atrophy
Disease Ontology
DOID:4751
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
23636 NUP62 nucleoporin 62
Displaying all 2 entries
Gene ID Gene Symbol Description Source
18226 Nup62 nucleoporin 62
234729 Vac14 Vac14 homolog (S. cerevisiae)
Displaying 1 entry
Gene ID Gene Symbol Description Source
65274 Nup62 nucleoporin 62
Displaying 1 entry
Gene ID Gene Symbol Description Source
36830 Nup62 Nucleoporin 62kD
Displaying 1 entry
Gene ID Gene Symbol Description Source
853409 NSP1 FG-nucleoporin NSP1
The Human Phenotype Ontology
Displaying entries 11 - 20 of 36 in total
HPO ID HPO Term
HP:0002376 Developmental regression
HP:0001260 Dysarthria
HP:0007340 Lower limb muscle weakness
HP:0001508 Failure to thrive
HP:0008947 Infantile muscular hypotonia
HP:0002066 Gait ataxia
HP:0001288 Gait disturbance
HP:0003484 Upper limb muscle weakness
HP:0000648 Optic atrophy
HP:0002359 Frequent falls
Displaying 1 entry
Gene ID Gene Symbol Description
103 ADAR adenosine deaminase RNA specific
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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

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Last updated: December 9, 2024