ORPHA:459537

Genetic complex vascular malformation with associated anomalies

Synonyms: Genetic hemangiolymphangioma

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	Genetic complex vascular malformation with associated anomalies	Genetic hemangiolymphangioma
fr	Malformation vasculaire complexe génétique avec anomalies associées	Hémangiolymphangiome d'origine génétique
de	Genetisch bedingte komplexe vaskuläre Fehlbildung mit assoziierten Anomalien	Hämangiolymphangiom, genetisch bedingtes
es	Malformación vascular genética compleja con anomalías asociadas	Hemangiolinfangioma genético
it	Malformazione vascolare genetica complessa associata ad anomalie
nl	Genetische complexe vasculaire malformatie met geassocieerde anomalieën	Genetisch hemangiolymfangioom
pt	Malformação vascular complexa genética com anomalias associadas
pl	Genetycznie uwarunkowana złożona malformacja naczyniowa z wadami towarzyszącymi	Hemangiolymfangioma
cs	Geneticky podmíněné komplexní vaskulární malformace s asociovanými anomáliemi	Genetický hemangiolymfangiom
uk	Генетично обумовлена складна судинна вада розвитку з супутніми аномаліями	Генетична гемангіолімфангіома
zh	遗传复杂血管畸形及相关异常	遗传性血管淋巴管瘤
tr	İlişkili anomaliler ile seyreden genetik kompleks vasküler malformasyon	Genetik hemanjiyolenfanjiyom

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
UMLS	C5679997	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:211240Genetic vascular anomaly
rare genetic diseases

Children (6):

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/459537
This record as JSON: /data/d/459537.json