Description
amyloidosis: A disorder characterized by the localized or diffuse accumulation of amyloid protein in various anatomic sites. It may be primary, due to clonal plasma cell proliferations; secondary, due to long standing infections, chronic inflammatory disorders, or malignancies; or familial. It may affect the nerves, skin, tongue, joints, heart, liver, spleen, kidneys and adrenal glands.
Data source
| FinnGen phenocode |
E4_METABOLIA |
| Include |
E4_AROMAMINO, E4_BRANCHAMINOFATAC, E4_AMINO, E4_LACTOSEINT, E4_CARBO, E4_SPHINGOLIP, E4_GLYCOSAMINOGLYC, E4_GLYCOPROT, E4_LIPOPROT, E4_PURINEPYRI, E4_PORBILIR, E4_MINERAL_MET, E4_CYSTFIBRO, E4_AMYLOIDOSIS, E4_VOLUME, E4_FLUIDELECTRO, E4_METABO |
| Level in the ICD-hierarchy |
2 |
| First defined in version |
DF2 |
Ontology