ICD-11 code : 5D00.2;
Preferred Label : Hereditary amyloidosis;
ICD-11 definition : 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.;
ICD-11 synonym : genetic amyloidosis; familial amyloidosis; Heredofamilial amyloidosis;
ICD-11 "other" category code : 5D00.2Y;
ICD-11 "unspecified" category code : 5D00.2Z;
Origin ID : 1152878652;
Currated CISMeF NLP mapping
- ICD-10 Mapping
- Validated automatic mappings to BTNT
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.
