raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:435603

Genetic otorhinolaryngological malformation

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.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enGenetic otorhinolaryngological malformation
frMalformation otorhinolaryngologique d'origine génétique
deOtorhinolaryngologische Fehlbildung, genetisch bedingte
esMalformación otorrinolaringológica genética
itMalformazione genetica d'interesse otorinolaringoiatrico
nlGenetische otorinolaryngologische malformatie
ptMalformação otorrinolaringológica genética
plMalformacja otorynolaryngologiczna uwarunkowana genetycznie
csGeneticky podmíněné otorinolaryngologické malformace
ukГенетично обумовлена оториноларингологічна вада розвитку
zh遗传性耳鼻喉科畸形
trGenetik kulak burun boğaz malformasyonu
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO18562Evalidated
UMLSC5681175Evalidated

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 (2):

Children (4):

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