ORPHA:217720

Non-familial restrictive cardiomyopathy

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	Non-familial restrictive cardiomyopathy
fr	Cardiomyopathie restrictive non familiale
de	Kardiomyopathie, restriktive, nicht-familiäre Form
es	Miocardiopatía restrictiva no familiar	Cardiomiopatía restrictiva no familiar
it	Cardiomiopatia restrittiva non familiare
nl	Niet-familiale restrictieve cardiomyopathie
pt	Miocardiopatia restritiva, não familiar
pl	Nierodzinna kardiomiopatia restrykcyjna
cs	Nefamiliární restriktivní kardiomyopatie
uk	Несімейна рестриктивна кардіоміопатія
zh	非家族性限制性心肌病
tr	Ailesel olmayan restriktif kardiyomiyopati

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
ICD-11	BC43.20	E	specific	validated
MONDO	0016345	E		validated
MONDO	16345	E		validated
UMLS	C5680885	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:97929Rare cardiac disease

Parents in the classifications (1):

ORPHA:217632Restrictive cardiomyopathy
rare cardiac diseases

Children (10):

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/217720
This record as JSON: /data/d/217720.json