Term Name: nuclear type mitochondrial complex I deficiency 25
Synonyms: MC1DN25
Definition: A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous and compound heterozygous mutation in the NDUFB3 gene on chromosome 2q33.1.
Ontology: Human Disease [DOID:0112067]   ( DOID:0112067 )

Relationships
is a type of: autosomal recessive disease nuclear type mitochondrial complex I deficiency