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
Disease Ontology
DOID:12704
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying all 7 entries
Gene ID Gene Symbol Description Source
472 ATM ATM serine/threonine kinase
545 ATR ATR serine/threonine kinase
581 BAX BCL2 associated X, apoptosis regulator
3458 IFNG interferon gamma
3558 IL2 interleukin 2
3569 IL6 interleukin 6
9759 HDAC4 histone deacetylase 4
Displaying all 4 entries
Gene ID Gene Symbol Description Source
12028 Bax BCL2-associated X protein
15978 Ifng interferon gamma
16183 Il2 interleukin 2
208727 Hdac4 histone deacetylase 4
Displaying all 2 entries
Gene ID Gene Symbol Description Source
25712 Ifng interferon gamma
116562 Il2 interleukin 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
181723 hda-4 Histone deacetylase 4

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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