Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition A rare, hereditary amyloidosis with primary renal involvement characterized by amyloid deposition in the kidney glomeruli and medulla, gastrointestinal tract, liver, spleen and slow disease progression. Symptoms and signs include nausea, vomiting, dyspepsia, gastritis, gastrointestinal hemorrhage, abdominal pain, hepatic rupture, sicca syndrome, purpura and petechiae, lymphadenopathy and renal dysfunction. Disease data Classification Clinical subtype Synonyms Familial amyloid nephropathy due to lysozyme variant Amyloidoza lizozymowa Dziedziczna amyloidoza nerek spowodowana wariantem lizozymu Dziedziczna nefropatia amyloidowa spowodowana wariantem lizozymu Rodzinna amyloidoza nerek spowodowana wariantem lizozymu Rodzinna nefropatia amyloidowa spowodowana wariantem lizozymu Familial renal amyloidosis due to lysozyme variant Hereditary amyloid nephropathy due to lysozyme variant Hereditary renal amyloidosis due to lysozyme variant Lysozyme amyloidosis ORPHA code 93561 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