Term Name: nuclear type mitochondrial complex I deficiency 27
Synonyms: MC1DN27
Definition: A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the MTFMT gene on chromosome 15q22.31.
Ontology: Human Disease [DOID:0112090]   ( DOID:0112090 )

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