Cardiomyopathy, Dilated, with Hypergonadotropic Hypogonadism (CMDHH)

Alias:

Malouf Syndrome

Najjar Syndrome

Dilated Cardiomyopathy-Hypergonadotropic Hypogonadism Syndrome

Cardiogenital Syndrome

Genital Anomaly with Cardiomyopathy

Cardiomyopathy with Primary Testicular Failure

Cardiomyopathy, Congestive, with Hypergonadotropic Hypogonadism

Congestive Cardiomyopathy with Hypergonadotropic Hypogonadism

Cardiomyopathy Congestive with Hypergonadotropic Hypogonadism

Cardiomyopathy, Diltaed, with Hypergonadotropic Hypogonadism

Dilated Cardiomyopathy with Hypergonadotropic Hypogonadism

Cardiomyopathy, Dilated, with Premature Ovarian Failure

Dilated Cardiomyopathy with Premature Ovarian Failure

Cardiomyopathy Dilated with Premature Ovarian Failure

Cardiomyopathy Eith Primary Testicular Failure

Cmdhh

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Cardiomyopathy, Dilated, with Hypergonadotropic Hypogonadism, also known as malouf syndrome, is related to crigler-najjar syndrome, type i and hutchinson-gilford progeria syndrome. An important gene associated with Cardiomyopathy, Dilated, with Hypergonadotropic Hypogonadism is LMNA (Lamin A/C), and among its related pathways/superpathways are Cell Cycle, Mitotic and Transport of the SLBP independent Mature mRNA. The drugs Carbamide peroxide and Liver Extracts have been mentioned in the context of this disorder. Affiliated tissues include heart and testes, and related phenotypes are ptosis and precocious puberty

Related ID：

MALACARDS：CRD229

OMIM：212112

MESH：C535580