Search Ontology:
Human Disease
dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome
- Term ID
- DOID:0111584
- Synonyms
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- 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
- Definition
- A syndrome characterized by dilated cardiomyopathy and hypergonadotropic hypogonadism that has_material_basis_in heterozygous mutation in the LMNA gene on chromosome 1q22. (2)
- References
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- GARD:3373
- MESH:C535580
- MESH:C535703
- MIM:212112
- NCI:C174217
- ORDO:2229
- SNOMEDCT_US_2023_03_01:719451006
- UMLS_CUI:C0796031
- UMLS_CUI:C0796083
- Ontology
- Human Disease ( DOID:0111584 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models