ORPHA:255225

OBSOLETE: Maternally-inherited mitochondrial hypertrophic cardiomyopathy

inactive · referred to ORPHA:254776Mitochondrial oxidative phosphorylation disorder due to a point mutation of mitochondrial DNA

Type: Disease
Group: Disorder
Status: inactive
Flag: Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Mitochondrial oxidative phosphorylation disorder due to a point mutation of mitochondrial DNA

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	OBSOLETE: Maternally-inherited mitochondrial hypertrophic cardiomyopathy
fr	OBSOLETE : Cardiomyopathie hypertrophique mitochondriale de transmission maternelle
de	OBSOLET: Kardiomyopathie, hypertrophe mitochondriale, maternal vererbte
es	OBSOLETO: Miocardiopatía hipertrófica mitocondrial de transmisión materna
it	OBSOLETO: Cardiomiopatia ipertrofica mitocondriale a trasmissione materna
nl	OBSOLEET: Maternaal overgeërfde mitochondriale hypertrofische cardiomyopathie
pt	OBSOLETO: Miocardiopatia hipertrófica mitocondrial com hereditariedade materna
pl	NIEAKTUALNE: Mitochondrialna kardiomiopatia przerostowa dziedziczona od matki
cs	NEAKTUÁLNÍ: Maternálně dědičná mitochondriální hypertrofická kardiomyopatie
uk	Успадкована по материнській лінії мітохондріальна гіпертрофічна кардіоміопатія
zh	弃用：母系遗传性线粒体肥厚性心肌病
tr	Eski adı: Maternal olarak kalıtsal mitokondriyal hipertrofik kardiyomiyopati

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

Classification

Not placed in any Orphanet classification in this release.

No children.

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/255225
This record as JSON: /data/d/255225.json