Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition A rare hereditary amyloidosis with primary renal involvement characterized by variable onset of renal insufficiency with edema, hypertension, proteinuria, and azotemia, eventually leading to end-stage renal disease. Amyloid cardiomyopathy and histopathological evidence of amyloid deposition in other organs, such as the spleen, liver, adrenal glands, and pancreas, among others, have also been described. Disease data Classification Clinical subtype Synonyms Apolipoprotein A-II amyloidosis Amyloidoza apolipoproteinowa A-II Dziedziczna amyloidoza nerek z powodu wariantu apolipoproteiny A-ll Dziedziczna nefropatia amyloidowa z powodu wariantu polipoproteiny A-ll Rodzinna amyloidoza nerek z powodu wariantu apolipoproteiny A-ll Rodzinna nefropatia amyloidowa z powodu wariantu apolipoproteiny A-ll Familial amyloid nephropathy due to apolipoprotein A-II variant Familial renal amyloidosis due to apolipoprotein A-II variant Hereditary amyloid nephropathy due to apolipoprotein A-II variant Hereditary renal amyloidosis due to apolipoprotein A-II variant ORPHA code 238269 OMIM code - ICD10 code E85.0 ICD11 code - *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl