raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:263324

Thymoma type AB

Type
Histopathological subtype
Group
Subtype of disorder
Inheritance
Not applicable
Age of onset
Adult
Status
active

This disease is described under Thymoma

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enThymoma type AB
frThymome type AB
deThymom Typ ABThymustumor, epithelialer primärer, Typ AB
esTimoma tipo AB
itTimoma tipo AB
nlThymoom type AB
ptTimoma tipo AB
plGrasiczak typu ABPierwotny guz nabłonkowy grasicy typu AB · Pierwotny nowotwór nabłonkowy grasicy typu AB
csThymom, typ ABPrimární epiteliální neoplázie thymu, typ AB · Primární epiteliální nádor thymu, typ AB
ukТимома, тип ABПервинне епітеліальне новоутворення тимуса, тип AB · Первинна епітеліальна пухлина тимуса, тип АВ
zhAB型胸腺瘤AB型原发性胸腺上皮肿瘤
trTimoma tipi ABPrimer timik epitelyal tümör tipAB · Primer timik epitelyal neoplazma tipAB
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10C37NTBTattributedvalidated
ICD-10D15.0NTBTattributedvalidated
ICD-112C27.2NTBTindexvalidated
ICD-11XH0JH0Especificvalidated
MONDO0016975Evalidated
UMLSC1266092Evalidated

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):

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

2 records
TypeClassValueAreaQualificationValidationSource
Annual incidence<1 / 1 000 000—EuropeClass onlyValidatedRARECARE surveillance of rare cancers in Europe 2011[OTHER]
Point prevalenceUnknown—WorldwideClass onlyNot yet validatedORPHANET

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