ORPHA:98727

Rare atrial defect and interatrial communication

Synonyms: Atrial defect and interauricular communication

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 atrial defect and interatrial communication	Atrial defect and interauricular communication
fr	Communication interatriale ou anomalie auriculaire rare	Communication interauriculaire ou anomalie auriculaire
de	Seltener Vorhofdefekt und interatriale Kommunikation	Vorhofdefekt und interaurikuläre Kommunikation
es	Defecto auricular y comunicación interauricular raros	Defecto auricular y comunicación interauricular
it	Difetto atriale e comunicazione interatriale
nl	Zeldzaam atriumdefect en interatriale communicatie	Atriumdefect en interauriculaire communicatie
pt	Defeito auricular raro e comunicação interauricular
pl	Wada przedsionka i połączenia międzyprzedsionkowego	= en
cs	Atriální defekty a interatriální komunikace	Atriální defekty a interaurikulární komunikace
uk	Рідкісні дефекти міжпредсердної перегородки та міжпередсердної комунікації	Дефект передсердь та міжаурикулярна комунікація
zh	罕见心房缺损和心房间连通	心房缺损并心耳间交通
tr	Nadir atriyal defekt ve interatriyal iletişim	Atriyal defekt ve interauriküler iletişim

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
UMLS	C5680337	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:88991Rare congenital heart disease
rare developmental anomalies during embryogenesis; rare cardiac malformations

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/98727
This record as JSON: /data/d/98727.json