OBO ID: DOID:0112099
Term Name: nuclear type mitochondrial complex I deficiency 12 Search Ontology:
Synonyms:
  • MC1DN12
Definition: A nuclear type mitochondrial complex I deficiency that has_material_basis_in hemizygous mutation in the NDUFA1 gene on chromosome Xq24. https://pubmed.ncbi.nlm.nih.gov/17262856/
References:
Ontology: Human Disease   ( DOID:0112099 )
Relationships
is a type of:
OTHER nuclear type mitochondrial complex I deficiency 12 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
NDUFA1 Mitochondrial complex I deficiency, nuclear type 12 301020
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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