OBO ID: DOID:0112139
Term Name: nuclear type mitochondrial complex I deficiency 35 Search Ontology:
Synonyms:
  • MC1DN35
Definition: A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in NDUFB10 on chromosome 16p13.3. https://pubmed.ncbi.nlm.nih.gov/28040730/
References:
Ontology: Human Disease   (DOID:0112139)
OTHER nuclear type mitochondrial complex I deficiency 35 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
NDUFB10 ?Mitochondrial complex I deficiency, nuclear type 35 619003
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None