Dilated Cardiomyopathy-Hypergonadotropic Hypogonadism Syndrome

**Semantic type:** Disease or Syndrome

**Definition:** An autosomal dominant condition caused by mutation(s) in the LMNA gene, encoding prelamin-A/C. It is characterized by dilated cardiomyopathy and hypergonadotropic hypogonadism.

**Synonyms:** - DCM-HH - Malouf Syndrome - Najjar Syndrome