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mitochondrial complex III deficiency nuclear type 8 | RareConnect | RareConnect.io

/mitochondrial complex III deficiency, nuclear type

/mitochondrial complex III deficiency nuclear type 8

mitochondrial complex III deficiency nuclear type 8

Rare Disease

MONDO:0014364

Also Known As

LYRM7 mitochondrial complex III deficiencymitochondrial complex III deficiency caused by mutation in LYRM7mitochondrial complex III deficiency nuclear type 8MC3DN8mitochondrial Complex 3 deficiency, nuclear type 8mitochondrial complex III deficiency, nuclear type 8

Definition

Any mitochondrial complex III deficiency in which the cause of the disease is a mutation in the LYRM7 gene.

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:615838 ↗

GARD

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