INFEVERS -- the Registry for FMF and hereditary inflammatory disorders mutations

What you can do:
Search for information on mutations responsible for hereditary inflammatory disorders in human.
Highlights:
  • The INFEVERS gateway provides researchers and clinicians with a common access location for information on similar diseases, allowing a rapid overview of the corresponding genetic defects at a glance.
  • The concerned hereditary inflammatory disorders include Familial Mediterranean Fever (FMF), TRAPS (TNF Receptor 1A Associated Syndrome), HIDS (HyperIgD Syndrome), MWS (Muckle-Wells Syndrome)/FCU (Familial Cold Urticaria)/CINCA (Chronic Infantile Neurological Cutaneous and Articular Syndrome).
Keywords:
  • hereditary inflammatory disorders
  • auto-inflammatory syndromes
  • Familial Mediterranean Fever
  • FMF
  • TRAPS
  • TNF Receptor 1A Associated Syndrome
  • HIDS
  • HyperIgD Syndrome
  • MWS
  • Muckle-Wells Syndrome
  • FCU
  • Familial Cold Urticaria
  • CINCA
  • Chronic Infantile Neurological Cutaneous and Articular Syndrome
  • human genetic disorders
  • human genetic diseases
  • literature reviews
  • literature studies
Literature & Tutorials:
PubMed Link: INFEVERS
This record last updated: 05-02-2005
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