raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:100021

Primary plasmacytoma of the bone

Type
Clinical subtype
Group
Subtype of disorder
Status
active

This disease is described under Plasmacytoma

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enPrimary plasmacytoma of the bone
frPlasmacytome primaire de l'os
dePlasmozytom, primäres, des Knochens
esPlasmacitoma primario del hueso
itPlasmocitoma primario dell'osso
nlPrimair plasmacytoom van bot
ptPlasmacitoma primário do osso
plPierwotny szpiczak mnogi kości
csPrimární plazmocytom kosti
ukПервинна плазмоцитома кістки
zh骨原发性浆细胞瘤
trKemiğin primer plazmasitomu
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10C90.3Especificvalidated
ICD-112A83.2NTBTindexvalidated
MONDO0015042Evalidated

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

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

  • ORPHA:86855Plasmacytoma
    rare neurological diseases; rare hematological diseases; rare neoplastic diseases; rare transplant-related disorders

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

1 record
TypeClassValueAreaQualificationValidationSource
Annual incidence1-9 / 1 000 0000.15 / 100 000United StatesValue and classValidated19016727[PMID]_SEER Surveillance Epidemiology and End Results 1992-2004[OTHER]

Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.

6

HPO phenotypes

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

7

Sources for this card