raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:1092

Renal-genital-middle ear anomalies

inactive · moved to ORPHA:2578Mayer-Rokitansky-Küster-Hauser syndrome type 2

Type
Malformation syndrome
Group
Disorder
Status
inactive
Flag
Deprecated entity

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Mayer-Rokitansky-Küster-Hauser syndrome type 2

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enRenal-genital-middle ear anomalies
frAnomalies rénales, génitales et de l'oreille moyenne
deAnomalien der Niere, Genitalien und des Mittelohrs
esAnomalías renales, genitales y de oído medio
itAnomalie renali, genitali e dell'orecchio medio
nlAnomalieën van nier-genitaliën-middenoor
ptAnomalias renais, genitais e do ouvido médio
plAnomalie nerek, narządów płciowych i ucha środkowego
csRenální-genitální-středoušní anomálie
ukАномалії нирок-геніталій-середнього вуха
zh肾-生殖器-中耳畸形
trRenal-genital-orta kulak anomalileri
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
OMIM267400Evalidated
UMLSC1849432Evalidated

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

3

Classification

Not placed in any Orphanet classification in this release.

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

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

7

Sources for this card