gray platelet syndrome

Summary
Synonym
  • BDPLT4
  • GPS
  • platelet alpha-granule deficiency
  • platelet-type bleeding disorder 4
Definition
A blood platelet disease characterized by selective deficiency in the number and contents of platelet alpha-granules, macrothrombocytopenia, enlarged platelets, myelofibrosis, splenomegaly, and increased bleeding time that has_material_basis_in homozygous or compound heterozygous mutation in the NBEAL2 gene on chromosome 3p21.
Super Class
autosomal recessive disease blood platelet disease
External Links
Disease Ontology
DOID:0111044
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
ORDO
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying entries 1 - 10 of 13 in total
Gene ID Gene Symbol Description Source
1738 DLD dihydrolipoamide dehydrogenase
3956 LGALS1 galectin 1
3964 LGALS8 galectin 8
4669 NAGLU N-acetyl-alpha-glucosaminidase
5319 PLA2G1B phospholipase A2 group IB
5320 PLA2G2A phospholipase A2 group IIA
6403 SELP selectin P
7412 VCAM1 vascular cell adhesion molecule 1
8398 PLA2G6 phospholipase A2 group VI
10855 HPSE heparanase

About Release Notes Help Feedback

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