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Human Disease

nuclear type mitochondrial complex I deficiency 29

Term ID
DOID:0112084
Synonyms
  • MC1DN29
Definition
A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the TMEM126B gene on chromosome 11q14.1. https://pubmed.ncbi.nlm.nih.gov/27374773/
References
Ontology
Human Disease   ( DOID:0112084 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models