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Human Disease

nuclear type mitochondrial complex I deficiency 10

Term ID
DOID:0112075
Synonyms
  • MC1DN10
Definition
A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFAF2 gene on chromosome 5q12.1. https://pubmed.ncbi.nlm.nih.gov/16200211/
References
Ontology
Human Disease   ( DOID:0112075 )
Relationships
is a type of
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Genes Involved
Zebrafish Models