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Dilated Cardiomyopathy-Hypergonadotropic Hypogonadism Syndrome (MONDO:0008915)

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

Overview

Category

Ontology ID

Internal:10178

Synonyms

Malouf syndrome

Najjar syndrome

cardiogenital syndrome

cardiomyopathy with primary testicular failure

cardiomyopathy, congestive, with hypergonadotropic hypogonadism

cardiomyopathy, dilated, with hypergonadotropic hypogonadism

cardiomyopathy, dilated, with premature ovarian failure

dilated cardiomyopathy with hypergonadotropic hypogonadism

genital anomaly with cardiomyopathy

Mapped terms

DOID:0111584

GARD:0003373

MEDGEN:162901

NCIT:C174217

OMIM:212112

Orphanet:2229

SCTID:719451006

UMLS:C0796031

Child terms

Unknown children.