ORPHA:717582

Coagulation abnormality associated with a vascular anomaly

Type: Clinical group
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

9 of 12 languages

Lang	Name	Synonyms
en	Coagulation abnormality associated with a vascular anomaly
fr	Anomalie de la coagulation associée à une anomalie vasculaire
de	Gerinnungsanomalie mit assoziierter Gefäßanomalie
es	Anomalía de la coagulación asociada a una anomalía vascular
it	Anomalia della coagulazione associata ad unanomalia vascolare
nl	Stollingsstoornis geassocieerd met een vasculaire anomalie	Stollingsafwijking geassocieerd met een vaatafwijking
pt	Coagulation abnormality associated with a vascular anomaly
pl	Nieprawidłowości krzepnięcia związane z anomalią naczyniową
cs	Coagulation abnormality associated with a vascular anomaly

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

Classification

Preferential parent (Orphanet linearisation):

ORPHA:98028Rare circulatory system disease

Parents in the classifications (1):

ORPHA:68419Rare vascular anomaly
rare developmental anomalies during embryogenesis; rare circulatory system diseases

Children (4):

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/717582
This record as JSON: /data/d/717582.json