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Human Disease

nuclear type mitochondrial complex I deficiency 9

Term ID
DOID:0112073
Synonyms
  • MC1DN9
Definition
A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFS6 gene on chromosome 5p15.33. https://pubmed.ncbi.nlm.nih.gov/15372108/
References
Ontology
Human Disease   ( DOID:0112073 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models