ORPHA:439246

ABeta2M amyloidosis

Synonyms: Beta2-microglobulinic amyloidosis

Type: Clinical group
Group: Group of disorders
Age of onset: Adult
Status: active

This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	ABeta2M amyloidosis	Beta2-microglobulinic amyloidosis
fr	Amylose ABeta2M	Amylose à bêta-2 microglobuline
de	ABeta2M-Amyloidose	Beta-2-Mikroglobulin-Amyloidose
es	Amiloidosis ABeta2M	Amiloidosis beta2-microglobulínica
it	Amiloidosi ABeta2M	Amiloidosi beta2-microglobulinica
nl	ABèta2M-amyloïdose	Bèta2-microglobuline-amyloïdose
pt	Amiloidose ABeta2M	Amiloidose beta2-microglobulínica
pl	Amyloidoza ABeta2M	Amyloidoza Beta2-mikroglobulinowa
cs	ABeta2M amyloidóza	Beta2-mikroglobulinemická amyloidóza
uk	Амілоїдоз ABeta2M	Бета2-мікроглобуліновий амілоїдоз
zh	ABeta2M淀粉样变性	Beta2-微球蛋白淀粉样变性
tr	ABeta2M amiloidoz	Beta2-mikroglobulinik amiloidozis

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
ICD-11	5D00.3	E	specific	validated
MONDO	0018590	E		validated
MONDO	18590	E		validated
UMLS	C5680053	E		validated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

Classification

Preferential parent (Orphanet linearisation):

ORPHA:98023Rare systemic or rheumatologic disease

Parents in the classifications (1):

ORPHA:69Amyloidosis
rare systemic and rheumatological diseases

Children (2):

Genes

0 direct

Orphanet records no gene directly on this code.

Prevalence and incidence

0 records

No prevalence record in this release.

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

Sources for this card

Orphanet page: orpha.net/en/disease/detail/439246
This record as JSON: /data/d/439246.json