raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:238642

Primary megaureter, adult-onset form

Type
Clinical subtype
Group
Subtype of disorder
Inheritance
Unknown
Age of onset
Adult
Status
active

This disease is described under Congenital primary megaureter

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enPrimary megaureter, adult-onset form
frMéga-uretère primitif de l'adulte
deMegaureter, primärer, adulte Form
esMegauréter primitivo del adulto
itMegauretere primitivo, forma a esordio nell'adulto
nlPrimaire mega-ureter, volwassen aanvang vorm
ptMegaureter primário, forma de início no adulto
plPierwotny moczowód olbrzymi, postać o początku w wieku dorosłym
csPrimární megaureter, adultní forma
ukПервинний мегауретер, що починається у дорослих
zh成人原发性巨输尿管
trPrimer megaüreter, yetişkin başlangıç ​​formu
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10Q62.2NTBTattributedvalidated
ICD-11LB31.1NTBTattributedvalidated
MONDO0016549Evalidated
UMLSC5680937Evalidated

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:617Congenital primary megaureter
    rare developmental anomalies during embryogenesis; rare genetic diseases; rare urogenital diseases; rare renal 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
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