raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:155832

Rare head and neck 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
enRare head and neck malformation
frMalformation rare de la tête et du cou
deKopf- und Nackenfehlbildung, seltene
esMalformación rara de cabeza y cuello
itMalformazione rara di testa e collo
nlZeldzame hoofd- en halsmalformatie
ptMalformação rara da cabeça e pescoço
plRzadkie malformacje głowy i szyi
csVzácné malformace hlavy a krku
ukРідкісна вада розвитку голови та шиї
zh罕见的头颈部畸形
trNadir baş ve boyun malformasyonu
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO15475Evalidated
UMLSC5680631Evalidated
GARD19972Evalidated

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):

Children (10):

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