Term Name: nuclear type mitochondrial complex I deficiency 28
Synonyms: MC1DN28
Definition: A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFA13 gene on chromosome 19p13.11.
Ontology: Human Disease [DOID:0112095]   ( DOID:0112095 )

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