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
External Links
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 1 - 10 of 22 in total
HPO ID HPO Term
HP:0003103 Abnormal cortical bone morphology
HP:0002167 Abnormality of speech or vocalization
HP:0006487 Bowing of the long bones
HP:0001744 Splenomegaly
HP:0004493 Craniofacial hyperostosis
HP:0002823 Abnormal femur morphology
HP:0000944 Abnormal metaphysis morphology
HP:0002992 Abnormal tibia morphology
HP:0005019 Diaphyseal undertubulation
HP:0001903 Anemia
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: August 19, 2024