ataxia telangiectasia (Q387082)

From Wikidata
Jump to navigation Jump to search
The printable version is no longer supported and may have rendering errors. Please update your browser bookmarks and please use the default browser print function instead.
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
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

Statements

0 references
0 references
0 references
0 references
Ataxia telangiectasia
0 references

Identifiers

0 references
0 references
0 references
0 references
0 references
0 references
0 references
0 references
0 references
0 references