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Human Disease

nuclear type mitochondrial complex I deficiency 25

Term ID
DOID:0112067
Synonyms
  • MC1DN25
Definition
A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous and compound heterozygous mutation in the NDUFB3 gene on chromosome 2q33.1. https://pubmed.ncbi.nlm.nih.gov/22277967/
References
Ontology
Human Disease   ( DOID:0112067 )
Relationships
is a type of
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Genes Involved
Zebrafish Models