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