MSeqDR Mitochondrial Disease Portal


 
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acquired amyloid peripheral neuropathy (MONDO:0016179)
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acquired metabolic disease (MONDO:0006504)
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amyloidosis (disease) (MONDO:0019065)
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non-familial restrictive cardiomyopathy (MONDO:0016345)
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secondary glomerular disease (MONDO:0019724)
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AA amyloidosis ()

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..expandAA amyloidosis ()
..expandAApoAIV amyloidosis ()
..expandadult-onset Still disease ()
..expandAH amyloidosis ()
..expandAL amyloidosis ()
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..expandautoimmune interstitial lung disease-arthritis syndrome ()
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..expandeosinophilic granulomatosis with polyangiitis ()
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..expandfamilial visceral amyloidosis ()
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..expandhypocomplementemic urticarial vasculitis ()
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..expandimmunoglobulin a vasculitis ()
..expandimmunotactoid or fibrillary glomerulopathy ()
..expandmicroscopic polyangiitis ()
..expandmixed connective tissue disease ()
..expandMuckle-Wells syndrome ()
..expandnon-amyloid monoclonal immunoglobulin deposition disease ()
..expandpauci-immune glomerulonephritis ()
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MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:19439
Name:AA amyloidosis
Definition:Secondary amyloidosis is a form of amyloidosis (see this term), that complicates chronic inflammatory disorders (mainly rheumatoid arthritis, see this term) and is characterized by the aggregation and deposition of amyloid fibrils composed of serum amyloid A protein, an acute phase reactant. Although spleen, suprarenal gland, liver and gut are frequent sites of amyloid deposition, the clinical picture is dominated by renal involvement.
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Synonyms:amyloid A amyloidosis; amyloidosis AA; inflammatory amyloidosis; reactive amyloidosis; secondary amyloidosis
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