ataxia telangiectasia

Summary
Synonym
  • Boder-Sedgwick syndrome
  • Louis Bar syndrome
Definition
An autosomal recessive cerebellar ataxia that is characterized by cerebellar ataxia, telangiectases, immune defects, and a predisposition to malignancy and that has_material_basis_in homozygous or compound heterozygous mutation in the ATM gene on chromosome 11q22.
Super Class
autosomal recessive cerebellar ataxia
External Links
Disease Ontology
DOID:12704
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying entries 11 - 20 of 25 in total
Gene ID Gene Symbol Description Source
4684 NCAM1 neural cell adhesion molecule 1
5168 ENPP2 ectonucleotide pyrophosphatase/phosphodiesterase 2
5290 PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha
5291 PIK3CB phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta
5293 PIK3CD phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta
5294 PIK3CG phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma
5321 PLA2G4A phospholipase A2 group IVA
5742 PTGS1 prostaglandin-endoperoxide synthase 1
6646 SOAT1 sterol O-acyltransferase 1
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