Term Name: nuclear type mitochondrial complex I deficiency 32
Synonyms: MC1DN32
Definition: A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFB8 gene on chromosome 10q24.31.
Ontology: Human Disease [DOID:0112080]   ( DOID:0112080 )

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