ORPHA:544578

Congenital primary megaureter, refluxing and 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, refluxing and obstructed form
fr	Méga-uretère primitif congénital obstructif et refluant	Méga-uretère primitif congénital obstructif avec reflux
de	Megaureter, kongenitaler primärer, obstruktive und refluxive Form
es	Megauréter congénito primario, forma refluyente y obstructiva
it	Megauretere congenito primitivo, forma refluente e ostruttiva
nl	Congenitale primaire mega-ureter, refluerende en obstructieve vorm
pt	Megaureter primário congénito, forma obstrutiva e de refluxo
pl	Wrodzony pierwotny moczowód olbrzymi, forma z refluksem i niedrożnością
cs	Vrozený primární megaureter, refluktující a obstrukční forma
uk	Вроджений первинний мегауретер, рефлюксна та обструктивна форма
zh	回流梗阻型先天性原发型巨输尿管
tr	Doğumsal primer megaüreter, reflü ve tıkalı form

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
ICD-10	Q62.2	NTBT	attributed	validated
MONDO	0035295	E		validated
UMLS	C5681326	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	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.