ID: 41

Disease Name: Familial Mediterranean Fever

Description: A group of hereditary autoinflammation diseases, characterized by recurrent fever, abdominal pain, headache, rash, pleurisy; and arthritis. Orchitis; benign meningitis; and amyloidosis may also occur. Homozygous or compound heterozygous mutations in marenostrin gene result in autosomal recessive transmission; simple heterozygous, autosomal dominant form of the disease.

Disease Type: Clinical conditions associated with amyloidosis

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

Tissue: Kidney

Cross References
https://meshb.nlm.nih.gov/record/ui?ui=D010505

https://www.omim.org/entry/249100

https://www.ncbi.nlm.nih.gov/pubmed/14022004

https://www.ncbi.nlm.nih.gov/pubmed/5056669

https://www.ncbi.nlm.nih.gov/pubmed/3966749

https://www.ncbi.nlm.nih.gov/pubmed/10211405

https://www.ncbi.nlm.nih.gov/pubmed/16284730

Alternative Names:
Benign Paroxysmal Peritonitis
Familial Mediterranean Fever, Autosomal Recessive
Familial Paroxysmal Polyserositis
Mediterranean Fever, Familial
Periodic Disease
Periodic Disease, Wolff's
Periodic Peritonitis
Polyserositis, Familial Paroxysmal
Polyserositis, Recurrent
Recurrent Polyserositis
Wolff Periodic Disease
Wolff's Periodic Disease 
FMF
Benign recurrent polyserositis

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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