Mitochondrial disease

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Mitochondrial disease with dilated cardiomyopathy

ORPHA:217613Category

What it is

Orphanet has not published a description for this disease yet. The identifiers, classification and cross-references below are still current.

Key facts

Classified as
Category

Genes reported in subtypes

MT-ATP8MT-CO1MT-CO2MT-CO3MT-CYBMT-ND1MT-ND3MT-ND4MT-ND5MT-ND6MT-RNR1MT-TFMT-THMT-TKMT-TL1MT-TPMT-TQMT-TS1MT-TS2MT-TWRRM2BTAFAZZIN

Orphanet records these genes on 6 more specific entries under this disorder, not on this entry itself:

A well-studied disease is usually split into subtypes, and the gene is curated on whichever one the evidence belongs to. Open a subtype to see which gene goes with it.

Cross-references

MONDO 16335UMLS C5680874

Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.

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