ORPHA:217598

Non-familial hypertrophic 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 hypertrophic cardiomyopathy
fr	Cardiomyopathie hypertrophique non familiale
de	Kardiomyopathie, hypertrophe, nicht-familiäre Form
es	Miocardiopatía hipertrófica no familiar	Cardiomiopatía hipertrófica no familiar
it	Cardiomiopatia ipertrofica non familiare
nl	Niet-familiale hypertrofische cardiomyopathie
pt	Miocardiopatia hipertrófica não familiar
pl	Nierodzinna kardiomiopatia przerostowa
cs	Nefamiliární hypertrofická kardiomyopatie
uk	Несімейна гіпертрофічна кардіоміопатія
zh	非家族性肥厚型心肌病
tr	Ailesel olmayan hipertrofik kardiyomiyopati

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	Validation
MONDO	0016330	E	validated
MONDO	16330	E	validated
UMLS	C5680883	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:217569Rare hypertrophic cardiomyopathy
rare cardiac diseases; rare transplant-related disorders

Children (2):

Codes that Orphanet moved or referred to this one:

ORPHA:217601OBSOLETE: Hypertrophic cardiomyopathy due to intensive athletic training referred to · inactive

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/217598
This record as JSON: /data/d/217598.json