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Human Disease

nuclear type mitochondrial complex I deficiency 30

Term ID
DOID:0112098
Synonyms
  • MC1DN30
Definition
A nuclear type mitochondrial complex I deficiency that has_material_basis_in hemizygous mutation in the NDUFB11 gene on chromosome Xp11.3. https://pubmed.ncbi.nlm.nih.gov/26741492/
References
Ontology
Human Disease   ( DOID:0112098 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models