A vast group of diseases defined by the presence of insoluble protein deposits in tissues. Amyloidoses are classified according to clinical signs and biochemical type of amyloid protein involved.

This is just here as a test because I lose it

Term information

database cross reference
  • UMLS:C0002726 (E (Exact mapping: the two concepts are equivalent))
  • ICD-10:E85.1 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
  • MeSH:D000686 (E (Exact mapping: the two concepts are equivalent))
  • ICD-10:E85.0 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
  • ICD-10:E85.8 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
  • ICD-10:E85.4 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
  • MedDRA:10002022 (E (Exact mapping: the two concepts are equivalent))
  • ICD-10:E85.3 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
  • ICD-10:E85.9 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
  • ICD-10:E85.2 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
hasDbXref

ICD-10:E85.4
ICD-10:E85.8
UMLS:C0002726
ICD-10:E85.9
MeSH:D000686
ICD-10:E85.0
ICD-10:E85.1
ICD-10:E85.2
MedDRA:10002022
ICD-10:E85.3

notation

ORPHA:69