ID: 64

Disease Name: Behcet Syndrome

Description: Rare chronic inflammatory disease involving the small blood vessels. It is of unknown etiology and characterized by mucocutaneous ulceration in the mouth and genital region and uveitis with hypopyon. The neuro-ocular form may cause blindness and death. Synovitis; thrombophlebitis; gastrointestinal ulcerations; retinal vasculitis; and optic atrophy may occur as well.

Disease Type: Clinical conditions associated with amyloidosis

ICD-10 Classification: Diseases of the Musculoskeletal System and Connective Tissue

Tissue: Kidney, Salivary Gland, Gastrointestinal Tract

Cross References
https://www.ncbi.nlm.nih.gov/pubmed/1147457

https://www.ncbi.nlm.nih.gov/pubmed/25579733

https://www.ncbi.nlm.nih.gov/pubmed/22961375

https://www.ncbi.nlm.nih.gov/pubmed/10644872

http://apps.who.int/classifications/icd10/browse/2016/en#/M35

https://meshb.nlm.nih.gov/record/ui?ui=D001528

https://www.omim.org/entry/109650

Alternative Names:
Adamantiades-Behcet Disease Complex
Behcet Disease
Behcet Triple Symptom Complex
Behcet's Syndrome
Old Silk Route Disease
Triple Symptom Complex
Triple-Symptom Complex
BD

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

//