nuclear type mitochondrial complex I deficiency 35

Term ID

DOID:0112139

Synonyms

• MC1DN35

Definition

A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFB10 gene on chromosome 16p13.3. https://pubmed.ncbi.nlm.nih.gov/28040730/

References

• OMIM:619003

Ontology

Human Disease   ( DOID:0112139 )