Disease #00523 (renal failure (renal failure))

Official abbreviation renal failure
Name renal failure
OMIM ID -
Inheritance -
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene APOA2
Associated tissues -
Disease features -
Remarks -


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00019882 - PubMed: De Gracia 2006 family, 6 affecteds (index, 4 sisters, nephew) M ? Spain Caucasian - 0 - - renal failure, amyloidosis, visceral (type VIII) nephrotic syndrome, renal biopsy, revealing renal amyloidosis (IHC excluded AA type ); echocardiogram, electromyogram and liver examination ruled out extra-renal involvement APOA2 APOA2 1 6 Johan den Dunnen
00019884 - PubMed: Yazaki 2001 - M ? United States Caucasian - 0 - - renal failure proteinuria; renal biopsy revealed amyloid deposition glomeruli APOA2 APOA2 1 1 Johan den Dunnen
00019885 - PubMed: Yazaki 2003 patient (father died of renal failure, paternal half brother has renal dysfunction) M - United States Armenian - 0 - - renal failure 34y-progressive renal dysfunction; 56y-amyloidosis on renal; echocardiogram showed mild intraventricular propeptides APOA2 APOA2 1 1 Johan den Dunnen
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