OBO ID: DOID:0112069
Term Name: nuclear type mitochondrial complex I deficiency 22 Search Ontology:
Synonyms:
  • MC1DN22
Definition: A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in NDUFA10 on chromosome 2q37.3. https://pubmed.ncbi.nlm.nih.gov/21150889/
References:
Ontology: Human Disease   (DOID:0112069)
OTHER nuclear type mitochondrial complex I deficiency 22 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
NDUFA10 Mitochondrial complex I deficiency, nuclear type 22 618243
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None