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Human Disease

nuclear type mitochondrial complex I deficiency 6

Term ID
DOID:0112066
Synonyms
  • MC1DN6
Definition
A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFS2 gene on chromosome 1q23. https://pubmed.ncbi.nlm.nih.gov/11220739/
References
Ontology
Human Disease   ( DOID:0112066 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models