autoimmune hemolytic anemia

Summary
Synonym
  • Autoimmune haemolytic anaemia
  • autoimmune hemolytic anaemia
Definition
An autoimmune disease of blood that is characterized by deficient red blood cells caused by auto-antibodies.
Super Class
autoimmune disease of blood hemolytic anemia
External Links
Disease Ontology
DOID:718
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying entries 1 - 10 of 11 in total
Gene ID Gene Symbol Description Source
28 ABO ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase
308 ANXA5 annexin A5
962 CD48 CD48 molecule
1604 CD55 CD55 molecule (Cromer blood group)
2215 FCGR3B Fc gamma receptor IIIb
3161 HMMR hyaluronan mediated motility receptor
4153 MBL2 mannose binding lectin 2
4860 PNP purine nucleoside phosphorylase
4952 OCRL OCRL inositol polyphosphate-5-phosphatase
10434 LYPLA1 lysophospholipase 1
Related Glycoprotein
Displaying entry 11 - 11 of 11 in total
UniProt ID Protein Name Source
Q9P2W7 Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 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 v4.0.0

Last updated: August 19, 2024