Ghosal hematodiaphyseal syndrome

Summary
Synonym
  • Ghosal hematodiaphyseal dysplasia
  • Ghosal syndrome
  • diaphyseal dysplasia-anemia syndrome
Definition
A syndrome characterized by increased bone density with predominant diaphyseal involvement and aregenerative corticosteroid-sensitive anemia that has_material_basis_in homozygous or compound heterozygous mutation in TBXAS1 on chromosome 7q34.
Super Class
autosomal recessive disease syndrome
Disease Ontology
DOID:0112251
Mondo Disease Ontology
ORDO
OMIM
GARD
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
6916 TBXAS1 thromboxane A synthase 1
The Human Phenotype Ontology
Displaying entries 21 - 22 of 22 in total
HPO ID HPO Term
HP:0100252 Diaphyseal dysplasia
HP:0005528 Bone marrow hypocellularity
Displaying 1 entry
Gene ID Gene Symbol Description
6916 TBXAS1 thromboxane A synthase 1

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024