ID: 56

Disease Name: Schnitzler Syndrome

Description: An extremely rare condition manifested as monoclonal immunoglobulin M dysproteinemia without features of lymphoproliferative disease, but with chronic urticaria, fever of unknown origin, disabling bone pain, hyperostosis, and increased erythrocyte sedimentation rate.

Disease Type: Clinical conditions associated with amyloidosis

ICD-10 Classification: Other

Tissue: Gastrointestinal Tract

Cross References
https://meshb.nlm.nih.gov/record/ui?ui=D019873

https://www.ncbi.nlm.nih.gov/pubmed/17586002

https://www.ncbi.nlm.nih.gov/pubmed/23619586

https://www.ncbi.nlm.nih.gov/pubmed/21143856

Alternative Names:
null

Precursor Proteins:
P0DJI8 | Serum amyloid A-1 protein
P0DJI9 | Serum amyloid A-2 protein


Co-deposited Proteins:
No information available



Link to Amyloidosis: 
	http://83.212.109.111:8084/amyco/29

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