ORPHA:238646

Congenital primary megaureter, obstructed form

This disease is described under Congenital primary megaureter

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Congenital primary megaureter, obstructed form
fr	Méga-uretère primitif obstructif congénital
de	Megaureter, kongenitaler primärer, obstruktiver Form
es	Megauréter primitivo congénito obstructivo
it	Megauretere primitivo congenito, forma ostruttiva
nl	Congenitale primaire mega-ureter, obstructieve vorm
pt	Megaureter primário congénito, forma com obstrução
pl	Wrodzony moczowód olbrzymi, postać przeszkodowa
cs	Vrozený primární megaureter, obstrukční forma
uk	Вроджений первинний мегауретер, непрохідна форма
zh	阻塞性先天性原发性巨输尿管
tr	Doğumsal primer megaüreter, tıkalı form

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
ICD-10	Q62.2	NTBT	attributed	validated
ICD-11	LB31.1	NTBT	index	validated
MONDO	0016550	E		validated
UMLS	C5680936	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):

ORPHA:617Congenital primary megaureter
rare developmental anomalies during embryogenesis; rare genetic diseases; rare urogenital diseases; rare renal diseases; rare transplant-related disorders

No children.

0 direct

Orphanet records no gene directly on this code.

1 record

Type	Class	Value	Area	Qualification	Validation	Source
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.