722292000: Autosomal dominant beta2-microglobulinic amyloidosis (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Viscus structure finding\Autosomal dominant beta2-microglobulinic amyloidosis
• \Disease\Genetic disease\Hereditary disease\Hereditary amyloidosis\Autosomal dominant beta2-microglobulinic amyloidosis
• \Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Autosomal dominant beta2-microglobulinic amyloidosis
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Autosomal dominant beta2-microglobulinic amyloidosis
• \Disease\Degenerative disorder\Amyloidosis\Hereditary amyloidosis\Autosomal dominant beta2-microglobulinic amyloidosis
• \Disease\Metabolic disease\Hereditary metabolic disease\Autosomal dominant beta2-microglobulinic amyloidosis

Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3331471014	Autosomal dominant beta2-microglobulinic amyloidosis (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3331472019	Autosomal dominant beta2-microglobulinic amyloidosis	en	Synonym	Active	Case insensitive	SNOMED CT core
3331473012	Variant ABeta2M amyloidosis	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3331474018	A form of amyloidosis with characteristics of the accumulation and extensive visceral deposition of beta 2 microglobulin leading to progressive gastrointestinal dysfunction, Sjögren syndrome and autonomic neuropathy.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start