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Human Disease

nuclear type mitochondrial complex I deficiency 35

Term ID
DOID:0112139
Synonyms
  • MC1DN35
Definition
A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFB10 gene on chromosome 16p13.3. https://pubmed.ncbi.nlm.nih.gov/28040730/
References
Ontology
Human Disease   ( DOID:0112139 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models