X-linked spinal muscular atrophy 2

Summary
Synonym
  • SMAX2
  • X-linked distal arthrogryposis multiplex congenita
  • X-linked spinal muscular atrophy type 2
  • infantile-onset X-linked spinal muscular atrophy
  • spinal muscular atrophy with arthrogryposis
Definition
A spinal muscular atrophy characterized by neonatal onset of severe hypotonia, areflexia, and multiple congenital contractures associated with loss of anterior horn cells and infantile death that has_material_basis_in hemizygous mutation in the UBA1 gene on chromosome Xp11.3.
Super Class
X-linked recessive disease spinal muscular atrophy
Disease Ontology
DOID:0111827
Mondo Disease Ontology
MeSH
UMLS
ORDO
OMIM
GARD
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
7317 UBA1 ubiquitin like modifier activating enzyme 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
22201 Uba1 ubiquitin-like modifier activating enzyme 1

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: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.1.0

Last updated: December 9, 2024