ORPHA:183533

Genetic multiple congenital anomalies/dysmorphic syndrome

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 multiple congenital anomalies/dysmorphic syndrome
fr	Anomalies congénitales multiples/syndrome dysmorphique d'origine génétique
de	Multiple kongenitale Anomalien/Dysmorphie-Syndrom, genetisch bedingt
es	Anomalías congénitas múltiples/síndrome dismórfico de origen genético
it	Sindrome genetica da anomalie/dismorfismi congeniti multipli
nl	Genetische meervoudige congenitale anomalieën/dysmorfiesyndroom
pt	Anomalias congénitas múltiplas genéticas/síndrome dismórfico
pl	Mnogie wady wrodzone uwarunkowane genetycznie/zespół dysmorficzny uwarunkowany genetycznie
cs	Geneticky podmíněné vrozené syndromy s mnohočetnými anomáliemi/dysmorfií
uk	Генетично обумовлені множинні вроджені аномалії/дисморфічний синдром
zh	遗传性多发性先天性遗传/异形综合征
tr	Genetik kompleks doğumsal anomaliler / dismorfik sendrom

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
UMLS	C5680558	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:183530Rare genetic developmental defect during embryogenesis
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/183533
This record as JSON: /data/d/183533.json