99967-2
Atypical hemolytic uremic syndrome multigene analysis in Blood or Tissue by Molecular genetics method
Active
Term Description
Multigene testing for atypical hemolytic uremic syndrome (aHUS), a condition that can begin in the neonatal period to adulthood and consists of hemolytic anemia, thrombocytopenia, and renal failure caused by platelet thrombi in the kidney and other organs. Genes associated with genetic aHUS include C3, C5, CD46, CFB, CFH, CFHR1, CFHR2, CFHR3, CFHR4, CFHR5, CFI, DGKE, PLG, THBD, and MMACHC. Testing is performed for diagnostic, prognostic, and therapeutic assessment in patients with aHUS.[NCBI Books: NBK1367]
Source: Regenstrief LOINC
Fully-Specified Name
- Component
- Atypical hemolytic uremic syndrome multigene analysis
- Property
- Find
- Time
- Pt
- System
- Bld/Tiss
- Scale
- Doc
- Method
- Molgen
Additional Names
- Short Name
- aHUS multigene analysis Bld/T
- Display Name
- Atypical hemolytic uremic syndrome multigene analysis Molgen Doc (Bld/Tiss)
- Consumer Name Alpha Get Info
- Atypical hemolytic uremic syndrome multigene analysis, Blood or tissue specimen
Basic Attributes
- Class
- MOLPATH
- Type
- Laboratory
- First Released
- Version 2.72
- Last Updated
- Version 2.72
- Order vs. Observation
- Both
Language Variants Get Info
Tag | Language | Translation |
---|---|---|
es-ES | Spanish (Spain) | Análisis multigénico del síndrome urémico hemolítico atípico: |
fr-FR | French (France) | Analyse multigénique d'un syndrome hémolytique urémique atypique: |
it-IT | Italian (Italy) | Analisi multigene della sindrome emolitico uremica atipica: Synonyms: Genetica molecolare Osservazione Patologia molecolare Punto nel tempo (episodio) Sangue Sangue o Tessuto Tessuto & |
nl-NL | Dutch (Netherlands) | multigen-analyse op atypisch hemolytisch-uremisch syndroom: Synonyms: aHUS; |
zh-CN | Chinese (China) | 非典型溶血性尿毒综合征多基因分析: Synonyms: 不典型 不典型的 临床文档型; |
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