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Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome

rare

A syndrome is characterized by the association of dilated cardiomyopathy and hypergonadotropic hypogonadism (DCM-HH).

Identifiers
MONDO:0008915 OMIM:212112Orphanet:2229
Causal genes
LMNA
Part of
Cardiogenetic diseaseEndocrine system disorderMale reproductive system disorder
Also known as
cardiogenital syndrome · dilated cardiomyopathy with hypergonadotropic hypogonadism · Malouf syndrome · Najjar syndrome

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