raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:79450

Non-hereditary congenital primary lymphedema

inactive · moved to ORPHA:79452Milroy disease

Type
Disease
Group
Disorder
Status
inactive
Flag
Deprecated entity

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Milroy disease

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enNon-hereditary congenital primary lymphedema
frLymphoedème primaire congénital non héréditaire
deLymphödem, kongenitales primäres, nicht-hereditäres
esLinfedema congénito primario no hereditario
itLinfedema primitivo congenito non ereditarioMalattia Milroy-simile
nlNiet-erfelijk congenitaal primair lymfoedeem
ptLinfedema primário congénito não-hereditário
plNiedziedziczny wrodzony pierwotny obrzęk limfatycznyChoroba podobna do choroby Milroy'a
csMilroy-like diseaseNonhereditární vrozený primární lymfedém · Onemocnění podobné Milroyově nemoci
ukНеспадкова вроджена первинна лімфедема
zh非遗传性先天性原发性淋巴水肿
trKalıtsal olmayan doğumsal primer lenfödem
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

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