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Human Disease

nuclear type mitochondrial complex I deficiency 22

Term ID
DOID:0112069
Synonyms
  • MC1DN22
Definition
A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFA10 gene on chromosome 2q37.3. https://pubmed.ncbi.nlm.nih.gov/21150889/
References
Ontology
Human Disease   ( DOID:0112069 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models