OBO ID: DOID:0112093
Term Name: nuclear type mitochondrial complex I deficiency 3 Search Ontology:
Synonyms:
  • MC1DN3
Definition: A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in NDUFS7 on chromosome 19p13.3. (2)
References:
Ontology: Human Disease   (DOID:0112093)
OTHER nuclear type mitochondrial complex I deficiency 3 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
NDUFS7 Mitochondrial complex I deficiency, nuclear type 3 618224
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None