Hereditary amyloidosis (Q40141): Difference between revisions

From determinar.ia.br - Determine suas informações
Created a new Item
 
Changed label, description and/or aliases in pt-br, en
description / pt-brdescription / pt-br
 
A amiloidose hereditária (amiloidose familiar) é uma doença hereditária que freqüentemente afeta o fígado, os nervos, o coração e os rins. Muitos tipos diferentes de anormalidades genéticas presentes ao nascimento estão associados a um risco aumentado de doença amilóide. O tipo e a localização de uma anormalidade no gene amilóide podem afetar o risco de certas complicações, a idade em que os sintomas aparecem pela primeira vez e a forma como a doença progride ao longo do tempo.
description / endescription / en
 
Hereditary amyloidosis (familial amyloidosis) is an inherited disorder that often affects the liver, nerves, heart and kidneys. Many different types of gene abnormalities present at birth are associated with an increased risk of amyloid disease. The type and location of an amyloid gene abnormality can affect the risk of certain complications, the age at which symptoms first appear, and the way the disease progresses over time.

Revision as of 05:50, 13 August 2026

Hereditary amyloidosis (familial amyloidosis) is an inherited disorder that often affects the liver, nerves, heart and kidneys. Many different types of gene abnormalities present at birth are associated with an increased risk of amyloid disease. The type and location of an amyloid gene abnormality can affect the risk of certain complications, the age at which symptoms first appear, and the way the disease progresses over time.
Language Label Description Also known as
default for all languages
5D00.2
    English
    Hereditary amyloidosis
    Hereditary amyloidosis (familial amyloidosis) is an inherited disorder that often affects the liver, nerves, heart and kidneys. Many different types of gene abnormalities present at birth are associated with an increased risk of amyloid disease. The type and location of an amyloid gene abnormality can affect the risk of certain complications, the age at which symptoms first appear, and the way the disease progresses over time.

      Statements