congenital dyserythropoietic anemia type Ib

Summary
Synonym
  • CDA, type Ib
  • CDAN1B
Definition
A congenital dyserythropoietic anemia type I that has_material_basis_in homozygous or compound heterozygous mutation in C15orf41 on chromosome 15q14.
Super Class
autosomal recessive disease congenital dyserythropoietic anemia type I
Disease Ontology
DOID:0111397
Mondo Disease Ontology
MeSH
UMLS
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
10483 SEC23B SEC23 homolog B, COPII coat complex component
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
Q15437 Protein transport protein Sec23B

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