Human Disease and Mouse Model Detail
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Human Disease
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Cardiomyopathy, Dilated, with Hypergonadotropic Hypogonadism
OMIM ID: 212112
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Synonyms
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Cardiogenital Syndrome;
Cardiomyopathy with Primary Testicular Failure;
Cardiomyopathy, Congestive, with Hypergonadotropic Hypogonadism;
Cardiomyopathy, Dilated, with Premature Ovarian Failure;
Genital Anomaly with Cardiomyopathy;
Malouf Syndrome;
Najjar Syndrome
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Genes and
mouse models
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Mutations in human and/or mouse homologs are associated with this disease
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*Gene is associated with the disease in this species |
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Lmna
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LMNA*
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1:1 Homology
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Analysis Tools