DISEASES

Disease-gene associations mined from literature

Human genes for Liddle syndrome

Liddle syndrome [DOID:0050477]

A lipid metabolism disorder that has_material_basis_in X-linked inheritance of the tafazzin gene and is characterized by decreased production of an enzyme required to produce cardiolipin.

Synonyms:  Liddle syndrome,  DOID:0050477,  Liddle disease,  Liddle disorder,  Liddle's syndrome ...

Linkouts:  OMIM