raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:137926

Primary laryngeal lymphangioma

Type
Malformation syndrome
Group
Disorder
Age of onset
Infancy, Neonatal
Status
active

Primary laryngeal lymphangioma is a rare, benign, congenital malformation of the lymphatic system characterized by a polypoidal, variable-sized, soft tissue mass located in the larynx. Most lesions manifest by the 2nd year of life and, depending on the size, patients may present with changes in voice, dysphagia, stridor, airway obstruction and/or respiratory distress. Cystic hygroma of the neck is frequently associated.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enPrimary laryngeal lymphangioma
frLymphangiome laryngé primaire
deLymphangiom, laryngeales, primäres
esLinfangioma primario de laringe
itLinfangioma primario della laringe
nlPrimair laryngeaal lymfangioom
ptLinfangioma laringeo primário
plPierwotny naczyniak chłonny krtani
csPrimární laryngeální lymfangiom
ukПервинна лімфангіома гортані
zh原发性喉淋巴管瘤
trPrimer laringeal lenfanjiyom

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10D18.1NTBTattributedvalidated
MONDO0015314Evalidated
UMLSC4706521Evalidated
GARD19891Evalidated

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):

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