Details of Disease

General Information of Disease (ID: DISW3YUD)

Disease Name Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome
Synonyms
cardiomyopathy, congestive, with hypergonadotropic hypogonadism; cardiomyopathy, dilated, with premature ovarian failure; cardiomyopathy, dilated, with hypergonadotropic hypogonadism; cardiomyopathy with primary testicular failure; dilated cardiomyopathy with hypergonadotropic hypogonadism; genital anomaly with cardiomyopathy; Malouf syndrome; Najjar syndrome; cardiogenital syndrome
Definition A syndrome is characterized by the association of dilated cardiomyopathy and hypergonadotropic hypogonadism (DCM-HH).
Disease Hierarchy
DISRGY2N: Endocrine disease
DISOEQW8: Male reproductive system disorder
DISMT2VZ: Cardiogenetic disease
DISW3YUD: Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome
Disease Identifiers
MONDO ID
MONDO_0008915
MESH ID
C535703
UMLS CUI
C0796031
OMIM ID
212112
MedGen ID
162901
Orphanet ID
2229

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 1 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
LMNA OT3SG7ZR Supportive Autosomal recessive [1]
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References

1 Ovarian failure and dilated cardiomyopathy due to a novel lamin mutation. Am J Med Genet A. 2009 Feb 15;149A(4):567-72. doi: 10.1002/ajmg.a.32627.