ORPHA:458830

Rare capillary malformation with associated anomalies

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	Rare capillary malformation with associated anomalies
fr	Malformation capillaire rare avec anomalies associées
de	Seltene kapilläre Fehlbildung mit assoziierten Anomalien
es	Malformación capilar rara con anomalías asociadas
it	Malformazione capillare con anomalie associate
nl	Zeldzame capillaire malformatie met geassocieerde anomalieën
pt	Malformação capilar com anomalias associadas
pl	Rzadka malformacja naczyniowa z wadami towarzyszącymi
cs	Vzácná kapilární malformace s asociovanými anomáliemi
uk	Рідкісна капілярна мальформація з супутніми аномаліями
zh	罕见毛细血管畸形及相关异常
tr	İlişkili anomaliler ile seyreden nadir kılcal damar malformasyonu

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
MONDO	18719	E		validated
UMLS	C5681120	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 (2):

ORPHA:211247Rare capillary malformation
rare developmental anomalies during embryogenesis; rare circulatory system diseases
ORPHA:459526Rare genetic capillary malformation
rare genetic diseases

Children (3):

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/458830
This record as JSON: /data/d/458830.json