GM1 gangliosidosis type 3

Summary
Synonym
  • adult-onset GM1 gangliosidosis
Definition
A GM1 gangliosidosis that is characterized by neurodegeneration and mild skeletal changes and with age at onset ranges from 3 to 30 years.
Super Class
GM1 gangliosidosis
Disease Ontology
DOID:0080489
Mondo Disease Ontology
ORDO
OMIM
GARD
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
2720 GLB1 galactosidase beta 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
12091 Glb1 galactosidase, beta 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
188583 bgal-1 Beta-galactosidase
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
P16278 Beta-galactosidase
The Human Phenotype Ontology
Displaying entries 11 - 20 of 29 in total
HPO ID HPO Term
HP:0000750 Delayed speech and language development
HP:0001744 Splenomegaly
HP:0001250 Seizure
HP:0001332 Dystonia
HP:0003274 Hypoplastic acetabulae
HP:0002650 Scoliosis
HP:0008166 Decreased beta-galactosidase activity
HP:0002240 Hepatomegaly
HP:0004322 Short stature
HP:0010729 Cherry red spot of the macula
Displaying 1 entry
Gene ID Gene Symbol Description
2720 GLB1 galactosidase beta 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