ORPHA:263317

Thymoma type B

This disease is described under Thymoma

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Thymoma type B
fr	Thymome type B
de	Thymom Typ B
es	Timoma tipo B
it	Timoma, tipo B	Neoplasia epiteliale primitiva del timo, tipo B · Tumore epiteliale primitivo del timo, tipo B
nl	Thymoom type B
pt	Timoma tipo B
pl	Grasiczak typu B	Pierwotny guz nabłonkowy grasicy typu B · Pierwotny nowotwór nabłonkowy grasicy typu B
cs	Thymom, typ B	Primární epiteliální neoplázie thymu, typ B · Primární epiteliální nádor thymu, typ B
uk	Тимома, тип В	Первинне епітеліальне новоутворення тимуса, тип В · Первинна епітеліальна пухлина тимуса, тип В
zh	B型胸腺瘤	B型原发性胸腺上皮性肿瘤
tr	Timoma tip B	Primer timik epitelyal tümör tipB · Primer timik epitelyal neoplazma tipB

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
ICD-10	C37	NTBT	attributed	validated
ICD-10	D15.0	NTBT	attributed	validated
ICD-11	2C27.2	NTBT	index	validated
MONDO	0016974	E		validated
UMLS	C1328042	E		validated

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

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

No children.

0 direct

Orphanet records no gene directly on this code.

2 records

Type	Class	Value	Area	Qualification	Validation	Source
Annual incidence	<1 / 1 000 000	—	Europe	Class only	Validated	RARECARE surveillance of rare cancers in Europe 2011[OTHER]
Point prevalence	Unknown	—	Worldwide	Class only	Not yet validated	ORPHANET

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

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