ataxia telangiectasia (Q387082)

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a rare, neurodegenerative, autosomal recessive human disease causing severe disability
  • Louis–Bar syndrome
  • Boder-Sedgwick syndrome
  • Louis Bar syndrome
  • ataxia telangiectasia syndrome
  • AT
  • At, Complementation Group C
  • ATAXIA-TELANGIECTASIA
  • ATAXIA-TELANGIECTASIA; AT
  • Ataxia Telangiectasia
  • Louis-Bar Syndrome
  • At, Complementation Group E
  • At1
  • At, Complementation Group a
  • Ataxia-Telangiectasia Variant
  • At, Complementation Group D
  • Immunodeficiency with ataxia telangiectasia
  • Cerebello-oculocutaneous telangiectasia
  • A–T
  • Ataxia–telangiectasia
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Language Label Description Also known as
English
ataxia telangiectasia
a rare, neurodegenerative, autosomal recessive human disease causing severe disability
  • Louis–Bar syndrome
  • Boder-Sedgwick syndrome
  • Louis Bar syndrome
  • ataxia telangiectasia syndrome
  • AT
  • At, Complementation Group C
  • ATAXIA-TELANGIECTASIA
  • ATAXIA-TELANGIECTASIA; AT
  • Ataxia Telangiectasia
  • Louis-Bar Syndrome
  • At, Complementation Group E
  • At1
  • At, Complementation Group a
  • Ataxia-Telangiectasia Variant
  • At, Complementation Group D
  • Immunodeficiency with ataxia telangiectasia
  • Cerebello-oculocutaneous telangiectasia
  • A–T
  • Ataxia–telangiectasia

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Ataxia telangiectasia
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