Term Name: nuclear type mitochondrial complex I deficiency 12
Synonyms: MC1DN12
Definition: A nuclear type mitochondrial complex I deficiency that has_material_basis_in hemizygous mutation in the NDUFA1 gene on chromosome Xq24.
Ontology: Human Disease [DOID:0112099]   ( DOID:0112099 )

Relationships
is a type of: nuclear type mitochondrial complex I deficiency X-linked recessive disease