Term Name: nuclear type mitochondrial complex I deficiency 24
Synonyms: MC1DN24
Definition: A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFB9 gene on chromosome 8q24.13.
Ontology: Human Disease [DOID:0112079]   ( DOID:0112079 )

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