Version: 8.0.0
Date: Tue Jan 28 2025
mitochondrial complex III deficiency nuclear type 8
DOID:0080117
SummaryAssociated GenesAssociated AllelesAssociated Models
Disease

mitochondrial complex III deficiency nuclear type 8

Definition
A mitochondrial complex III deficiency characterized by childhood onset of progressive neurodegeneration that has_material_basis_in homozygous mutation in the LYRM7 gene on chromosome 5q23.
Synonyms
None
Cross References
Parent Terms
Child Terms
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Sources of Associations

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    Associated Alleles

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      Associated Models

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