ORPHA:182121

Non-syndromic urogenital tract malformation of male

Type: Category
Group: Group of disorders
Status: active

This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Non-syndromic urogenital tract malformation of male
fr	Malformation urogénitale non syndromique de l'homme
de	Urogenitale Fehlbildungen, männliche, nichtsyndromale Formen
es	Malformación no sindrómica del tracto urogenital masculino
it	Malformazione non sindromica dell'apparato urogenitale maschile
nl	Niet-syndromale malformatie van urogenitaal systeem van man
pt	Malformação do trato genito-urinário masculino não sindromática
pl	Niesyndromiczna malformacja męskiego układu moczowo-płciowego
cs	Nesyndromické malformace urogenitálního traktu mužů
uk	Несиндромальна вада розвитку сечостатевої системи у чоловіків
zh	男性非综合征性泌尿生殖道畸形
tr	Erkekte non-endromik ürogenital sistem malformasyonu

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
MONDO	15933	E		validated
UMLS	C5680593	E		validated

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

Classification

Preferential parent (Orphanet linearisation):

ORPHA:93890Rare developmental defect during embryogenesis

Parents in the classifications (1):

ORPHA:165704Non-syndromic urogenital tract malformation
rare developmental anomalies during embryogenesis; rare urogenital diseases; rare transplant-related disorders

Children (8):

Genes

0 direct

Orphanet records no gene directly on this code.

Prevalence and incidence

0 records

No prevalence record in this release.

HPO phenotypes

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

Sources for this card

Orphanet page: orpha.net/en/disease/detail/182121
This record as JSON: /data/d/182121.json