ORPHA:568041

Primary lymphedema without systemic or visceral involvement

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.

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Primary lymphedema without systemic or visceral involvement
fr	Lymphoedème primaire sans atteinte systémique ou viscérale
de	Primäres Lymphödem ohne systemische und viszerale Beteiligung
es	Linfedema primario sin afectación sistémica o visceral
it	Linfedema primitivo non sistemico o viscerale
nl	Primair lymfoedeem zonder systemische of viscerale betrokkenheid
pt	Linfedema primário sem envolvimento sistémico ou visceral
pl	Pierwotny obrzęk limfatyczny bez zmian układowych lub trzewnych
cs	Primární lymfedém bez systémového nebo viscerálního postižení
uk	Первинна лімфедема без системного або вісцерального ураження
zh	无全身或内脏受累型原发性淋巴水肿
tr	Sistemik veya viseral tutulum olmayan primer lenfödem

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
UMLS	C5681302	E		validated

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

Classification

Preferential parent (Orphanet linearisation):

ORPHA:93890Rare developmental defect during embryogenesis

Parents in the classifications (1):

ORPHA:77240Primary lymphedema
rare developmental anomalies during embryogenesis; rare genetic diseases; rare skin diseases; rare circulatory system diseases

Children (2):

Genes

0 direct

Orphanet records no gene directly on this code.

Prevalence and incidence

0 records

No prevalence record in this release.

HPO phenotypes

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

Sources for this card

Orphanet page: orpha.net/en/disease/detail/568041
This record as JSON: /data/d/568041.json