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dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome (DOID:0111584)
Alliance: disease page
Synonyms: cardiogenital syndrome; cardiomyopathy eith primary testicular failure; congestive cardiomyopathy with hypergonadotropic hypogonadism; dilated cardiomyopathy with hypergonadotropic hypogonadism; dilated cardiomyopathy with premature ovarian failure; genital anomaly with cardiomyopathy; Malouf syndrome; Najjar syndrome
Alt IDs: OMIM:212112, MESH:C535580, MESH:C535703, NCI:C174217, ORDO:2229, UMLS_CUI:C0796031, UMLS_CUI:C0796083
Definition: A syndrome characterized by dilated cardiomyopathy and hypergonadotropic hypogonadism that has_material_basis_in heterozygous mutation in LMNA on chromosome 1q22.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
09/27/2022
MGI 6.21
The Jackson Laboratory