Term Name: nuclear type mitochondrial complex I deficiency 30
Synonyms: MC1DN30
Definition: A nuclear type mitochondrial complex I deficiency that has_material_basis_in hemizygous mutation in the NDUFB11 gene on chromosome Xp11.3.
Ontology: Human Disease [DOID:0112098]   ( DOID:0112098 )

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